NRCAM (neuronal cell adhesion molecule) - Rat Genome Database

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Gene: NRCAM (neuronal cell adhesion molecule) Homo sapiens
Analyze
Symbol: NRCAM
Name: neuronal cell adhesion molecule
RGD ID: 731343
HGNC Page HGNC:7994
Description: Enables ankyrin binding activity. Involved in angiogenesis; central nervous system development; and clustering of voltage-gated sodium channels. Predicted to be located in axon initial segment. Predicted to be active in axon; glutamatergic synapse; and postsynaptic density membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: bravo; hBravo; KIAA0343; MGC138845; MGC138846; NEDNMS; neuron-glia-cam-related cell adhesion molecule; neuronal surface protein Bravo; ng-CAM-related; NgCAM-related cell adhesion molecule; nr-CAM; NrCAM-
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387108,147,649 - 108,456,720 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7108,147,623 - 108,456,717 (-)EnsemblGRCh38hg38GRCh38
GRCh377107,788,094 - 108,097,164 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 367107,575,318 - 107,884,062 (-)NCBINCBI36Build 36hg18NCBI36
Build 347107,382,057 - 107,690,734NCBI
Celera7102,595,073 - 102,910,207 (-)NCBICelera
Cytogenetic Map7q31.1NCBI
HuRef7102,150,368 - 102,465,060 (-)NCBIHuRef
CHM1_17107,721,788 - 108,030,155 (-)NCBICHM1_1
T2T-CHM13v2.07109,465,793 - 109,781,370 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27107,149,256 - 107,464,062 (-)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,2-dimethylhydrazine  (ISO)
17beta-estradiol  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP)
2-methylcholine  (EXP)
3,3',5,5'-tetrabromobisphenol A  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
4,4'-sulfonyldiphenol  (EXP)
4-(N-nitrosomethylamino)-1-(3-pyridyl)butan-1-one  (ISO)
5-aza-2'-deoxycytidine  (EXP)
6-propyl-2-thiouracil  (ISO)
8-Br-cAMP  (EXP)
acetamide  (ISO)
acetylsalicylic acid  (EXP)
acrylamide  (ISO)
aflatoxin B1  (EXP,ISO)
all-trans-retinoic acid  (EXP,ISO)
alpha-Zearalanol  (ISO)
ammonium chloride  (ISO)
androgen antagonist  (ISO)
anthracen-2-amine  (ISO)
antimycin A  (EXP)
aristolochic acid A  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
azoxystrobin  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[b]fluoranthene  (ISO)
bis(2-ethylhexyl) phthalate  (EXP,ISO)
bisphenol A  (EXP,ISO)
Bisphenol B  (EXP)
bisphenol F  (EXP)
butanal  (EXP)
Butylparaben  (ISO)
cadmium dichloride  (ISO)
caffeine  (EXP)
carbon nanotube  (ISO)
CGP 52608  (EXP)
chloroprene  (ISO)
chlorpyrifos  (ISO)
chrysene  (ISO)
clotrimazole  (ISO)
cobalt dichloride  (EXP)
copper atom  (EXP,ISO)
copper(0)  (EXP,ISO)
coumestrol  (EXP)
Cuprizon  (ISO)
cyclosporin A  (EXP)
cyproconazole  (ISO)
DDE  (ISO)
decabromodiphenyl ether  (ISO)
deguelin  (EXP)
dexamethasone  (EXP)
dibutyl phthalate  (ISO)
dorsomorphin  (EXP)
endosulfan  (ISO)
Enterolactone  (EXP)
entinostat  (EXP)
enzacamene  (ISO)
epoxiconazole  (ISO)
ethanol  (EXP,ISO)
fenpyroximate  (EXP)
flavonoids  (ISO)
FR900359  (EXP)
fulvestrant  (EXP)
gold atom  (EXP)
gold(0)  (EXP)
Heliotrine  (ISO)
hexaconazole  (ISO)
hydrogen peroxide  (EXP)
indometacin  (EXP)
Lasiocarpine  (ISO)
lead(0)  (EXP)
linuron  (ISO)
lithium chloride  (ISO)
methimazole  (ISO)
methylmercury chloride  (EXP)
mono(2-ethylhexyl) phthalate  (ISO)
morphine  (ISO)
N-nitrosomorpholine  (ISO)
nickel atom  (EXP)
ozone  (ISO)
paracetamol  (ISO)
PD 0325901  (EXP)
perfluorononanoic acid  (EXP)
perfluorooctanoic acid  (ISO)
phenytoin  (ISO)
picoxystrobin  (EXP)
pirinixic acid  (ISO)
potassium dichromate  (ISO)
prochloraz  (ISO)
procymidone  (ISO)
Ptaquiloside  (ISO)
pyrimidifen  (EXP)
sarin  (EXP)
SB 431542  (EXP)
senecionine  (ISO)
Senkirkine  (ISO)
serpentine asbestos  (ISO)
silicon dioxide  (EXP)
sodium arsenate  (EXP)
sodium arsenite  (EXP,ISO)
tebufenpyrad  (EXP)
temozolomide  (EXP)
testosterone  (ISO)
tetraphene  (ISO)
thifluzamide  (EXP)
thioacetamide  (ISO)
titanium dioxide  (ISO)
trichloroethene  (ISO)
trichostatin A  (EXP)
triclosan  (EXP)
triptonide  (ISO)
tunicamycin  (EXP)
urethane  (EXP)
valproic acid  (EXP,ISO)
vanadium atom  (EXP)
vanadium(0)  (EXP)
vinclozolin  (ISO)
zoledronic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Acetabular dysplasia  (IAGP)
Aggressive behavior  (IAGP)
Arachnoid cyst  (IAGP)
Ataxia  (IAGP)
Autosomal recessive inheritance  (IAGP)
Cataract  (IAGP)
Cerebral palsy  (IAGP)
Coarse facial features  (IAGP)
Colpocephaly  (IAGP)
Congenital onset  (IAGP)
Coxa valga  (IAGP)
Deep philtrum  (IAGP)
Delayed CNS myelination  (IAGP)
Demyelinating peripheral neuropathy  (IAGP)
Depressed nasal bridge  (IAGP)
Distal arthrogryposis  (IAGP)
Early young adult onset  (IAGP)
Exaggerated cupid's bow  (IAGP)
Failure to thrive  (IAGP)
Gastroesophageal reflux  (IAGP)
Gastrostomy tube feeding in infancy  (IAGP)
Global developmental delay  (IAGP)
Hammertoe  (IAGP)
Hearing impairment  (IAGP)
High myopia  (IAGP)
High palate  (IAGP)
Hip dysplasia  (IAGP)
Hydrocephalus  (IAGP)
Hypertelorism  (IAGP)
Hypotonia  (IAGP)
Intellectual disability  (IAGP)
Intrauterine growth retardation  (IAGP)
Irritability  (IAGP)
Jaw hyperreflexia  (IAGP)
Juvenile onset  (IAGP)
Laryngomalacia  (IAGP)
Long eyelashes  (IAGP)
Long face  (IAGP)
Medial flaring of the eyebrow  (IAGP)
Microcephaly  (IAGP)
Micrognathia  (IAGP)
Motor delay  (IAGP)
Narrow forehead  (IAGP)
Optic atrophy  (IAGP)
Periorbital fullness  (IAGP)
Periventricular heterotopia  (IAGP)
Periventricular leukomalacia  (IAGP)
Pes cavus  (IAGP)
Plagiocephaly  (IAGP)
Pleomorphic xanthoastrocytoma  (IAGP)
Polyhydramnios  (IAGP)
Posteriorly rotated ears  (IAGP)
Retinal detachment  (IAGP)
Scoliosis  (IAGP)
Self-injurious behavior  (IAGP)
Short chin  (IAGP)
Short nose  (IAGP)
Short stature  (IAGP)
Strabismus  (IAGP)
Tented upper lip vermilion  (IAGP)
Thick eyebrow  (IAGP)
Thin corpus callosum  (IAGP)
Upslanted palpebral fissure  (IAGP)
Ventriculomegaly  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8812479   PMID:8889548   PMID:8922386   PMID:9049255   PMID:9205841   PMID:9321706   PMID:9604207   PMID:11449000   PMID:11483367   PMID:11724816   PMID:11866539   PMID:12045112  
PMID:12139915   PMID:12183361   PMID:12421765   PMID:12477932   PMID:12853948   PMID:14602817   PMID:14702039   PMID:15128462   PMID:15523497   PMID:16123759   PMID:16335952   PMID:16344560  
PMID:17106428   PMID:17667921   PMID:18602664   PMID:18664314   PMID:19058789   PMID:19086053   PMID:19154219   PMID:19598235   PMID:20039944   PMID:20379614   PMID:20602751   PMID:21718388  
PMID:21873635   PMID:21876539   PMID:22182708   PMID:22889411   PMID:23338556   PMID:23593202   PMID:23897819   PMID:24366813   PMID:24667918   PMID:25798074   PMID:25921289   PMID:27732334  
PMID:29507755   PMID:30076541   PMID:30631154   PMID:31322225   PMID:32460013   PMID:32588424   PMID:33961781   PMID:34349018   PMID:35108495   PMID:35220890   PMID:35763884   PMID:35831314  
PMID:35914814   PMID:36181733   PMID:36215168   PMID:37993901   PMID:38485895  


Genomics

Comparative Map Data
NRCAM
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387108,147,649 - 108,456,720 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7108,147,623 - 108,456,717 (-)EnsemblGRCh38hg38GRCh38
GRCh377107,788,094 - 108,097,164 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 367107,575,318 - 107,884,062 (-)NCBINCBI36Build 36hg18NCBI36
Build 347107,382,057 - 107,690,734NCBI
Celera7102,595,073 - 102,910,207 (-)NCBICelera
Cytogenetic Map7q31.1NCBI
HuRef7102,150,368 - 102,465,060 (-)NCBIHuRef
CHM1_17107,721,788 - 108,030,155 (-)NCBICHM1_1
T2T-CHM13v2.07109,465,793 - 109,781,370 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27107,149,256 - 107,464,062 (-)NCBI
Nrcam
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391244,375,568 - 44,651,977 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1244,375,668 - 44,648,747 (+)EnsemblGRCm39 Ensembl
GRCm381244,328,786 - 44,605,194 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1244,328,885 - 44,601,964 (+)EnsemblGRCm38mm10GRCm38
MGSCv371245,429,872 - 45,702,833 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361245,199,270 - 45,469,127 (+)NCBIMGSCv36mm8
Celera1245,683,540 - 45,966,316 (+)NCBICelera
Cytogenetic Map12B2NCBI
cM Map1220.71NCBI
Nrcam
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8667,129,723 - 67,425,510 (+)NCBIGRCr8
mRatBN7.2661,402,813 - 61,698,536 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl661,329,863 - 61,702,992 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx661,738,687 - 62,028,234 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0662,053,678 - 62,343,220 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0661,526,131 - 61,817,117 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0664,297,843 - 64,867,408 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl664,297,888 - 64,864,996 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0673,887,250 - 74,029,039 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Rnor_5.0674,371,672 - 74,446,689 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4663,717,460 - 64,015,522 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1663,720,585 - 64,018,648 (+)NCBI
Celera660,398,331 - 60,686,704 (+)NCBICelera
Cytogenetic Map6q21NCBI
Nrcam
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541012,437,248 - 12,518,075 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541012,437,248 - 12,518,083 (-)NCBIChiLan1.0ChiLan1.0
NRCAM
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v26144,993,564 - 145,307,040 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan17193,263,534 - 193,577,010 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v07100,129,389 - 100,442,910 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.17112,849,823 - 113,107,008 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl7112,849,811 - 112,942,413 (-)Ensemblpanpan1.1panPan2
NRCAM
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11812,264,063 - 12,477,247 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1812,264,063 - 12,475,230 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1811,846,533 - 12,121,649 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01812,473,514 - 12,748,839 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1812,473,516 - 12,748,837 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11812,290,622 - 12,565,756 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01812,211,034 - 12,486,329 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01812,438,363 - 12,713,835 (+)NCBIUU_Cfam_GSD_1.0
Nrcam
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440511868,015,682 - 68,287,622 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366531,169,177 - 1,238,140 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366531,167,055 - 1,238,241 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NRCAM
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl9107,928,866 - 108,247,593 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.19107,928,866 - 108,248,018 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.29118,693,386 - 118,788,883 (-)NCBISscrofa10.2Sscrofa10.2susScr3
NRCAM
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12177,065,496 - 77,370,774 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2177,065,211 - 77,270,797 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604226,492,852 - 26,798,704 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Nrcam
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462473921,308,457 - 21,633,627 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NRCAM
81 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 copy number gain not provided [RCV000682911] Chr7:98693388..159119707 [GRCh37]
Chr7:7q22.1-36.3		 pathogenic
NM_001037132.4(NRCAM):c.2925G>A (p.Pro975=) single nucleotide variant NRCAM-related condition [RCV003939422] Chr7:108178039 [GRCh38]
Chr7:107818484 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001037132.4(NRCAM):c.1357C>G (p.Pro453Ala) single nucleotide variant NRCAM-related condition [RCV003939479] Chr7:108195867 [GRCh38]
Chr7:107836311 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001037132.4(NRCAM):c.2036-21GT[5] microsatellite NRCAM-related condition [RCV003941366] Chr7:108184624..108184625 [GRCh38]
Chr7:107825068..107825069 [GRCh37]
Chr7:7q31.1		 likely benign
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
NC_000007.13:g.(20954043_21001537)_(114528369_114556605)inv inversion Childhood apraxia of speech [RCV000234948] Chr7:21001537..114528369 [GRCh37]
Chr7:7p15.3-q31.1		 pathogenic
GRCh38/hg38 7q22.3-31.1(chr7:106261939-111228036)x1 copy number loss See cases [RCV000054158] Chr7:106261939..111228036 [GRCh38]
Chr7:105902385..110868092 [GRCh37]
Chr7:105689621..110655328 [NCBI36]
Chr7:7q22.3-31.1		 pathogenic
GRCh38/hg38 7q22.1-31.1(chr7:101807149-112414850)x1 copy number loss See cases [RCV000050924] Chr7:101807149..112414850 [GRCh38]
Chr7:101450429..112054905 [GRCh37]
Chr7:101237149..111842141 [NCBI36]
Chr7:7q22.1-31.1		 pathogenic
NM_001193582.1(NRCAM):c.1537C>T (p.Pro513Ser) single nucleotide variant Malignant melanoma [RCV000067579] Chr7:108194355 [GRCh38]
Chr7:107834799 [GRCh37]
Chr7:107622035 [NCBI36]
Chr7:7q31.1		 not provided
NM_001037132.4(NRCAM):c.3764T>G (p.Leu1255Arg) single nucleotide variant not provided [RCV000087187] Chr7:108150061 [GRCh38]
Chr7:107790506 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 copy number gain See cases [RCV000136717] Chr7:97419852..158923762 [GRCh38]
Chr7:97049164..158716453 [GRCh37]
Chr7:96887100..158409214 [NCBI36]
Chr7:7q21.3-36.3		 pathogenic
GRCh38/hg38 7q22.1-31.31(chr7:102196924-121278641)x1 copy number loss See cases [RCV000137522] Chr7:102196924..121278641 [GRCh38]
Chr7:101912320..120918695 [GRCh37]
Chr7:101626924..120705931 [NCBI36]
Chr7:7q22.1-31.31		 pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
NM_001037132.4(NRCAM):c.2043C>A (p.Ile681=) single nucleotide variant NRCAM-related condition [RCV003896464] Chr7:108184607 [GRCh38]
Chr7:107825051 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001037132.4(NRCAM):c.-331-26289_-331-18537del deletion Normal pregnancy [RCV000161491] Chr7:108418130..108425882 [GRCh38]
Chr7:108058574..108066326 [GRCh37]
Chr7:7q31.1		 not provided
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 copy number gain See cases [RCV000447709] Chr7:98969247..159119707 [GRCh37]
Chr7:7q22.1-36.3		 pathogenic
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34		 pathogenic
NM_001037132.4(NRCAM):c.1770T>C (p.Ser590=) single nucleotide variant NRCAM-related condition [RCV003949374] Chr7:108194032 [GRCh38]
Chr7:107834476 [GRCh37]
Chr7:7q31.1		 likely benign
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q31.1(chr7:107960937-108027226)x1 copy number loss not provided [RCV000746962] Chr7:107960937..108027226 [GRCh37]
Chr7:7q31.1		 benign
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
NM_001037132.4(NRCAM):c.2411C>G (p.Ser804Cys) single nucleotide variant High myopia [RCV000785731] Chr7:108182814 [GRCh38]
Chr7:107823258 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
NM_001037132.4(NRCAM):c.3598+8A>G single nucleotide variant not provided [RCV000915204] Chr7:108160353 [GRCh38]
Chr7:107800798 [GRCh37]
Chr7:7q31.1		 likely benign
GRCh37/hg19 7q31.1(chr7:107786826-112356275)x1 copy number loss not provided [RCV000847183] Chr7:107786826..112356275 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2699A>G (p.Glu900Gly) single nucleotide variant NRCAM-related condition [RCV003916122]|not provided [RCV000963354] Chr7:108180375 [GRCh38]
Chr7:107820819 [GRCh37]
Chr7:7q31.1		 likely benign
GRCh37/hg19 7q31.1-31.31(chr7:107410314-117825549)x1 copy number loss not provided [RCV000846765] Chr7:107410314..117825549 [GRCh37]
Chr7:7q31.1-31.31		 pathogenic
NM_001037132.4(NRCAM):c.1147A>C (p.Arg383=) single nucleotide variant NRCAM-related condition [RCV003897956]|not provided [RCV000970990] Chr7:108207588 [GRCh38]
Chr7:107848032 [GRCh37]
Chr7:7q31.1		 benign
NM_001037132.4(NRCAM):c.2289G>A (p.Leu763=) single nucleotide variant NRCAM-related condition [RCV003913109]|not provided [RCV000923572] Chr7:108184256 [GRCh38]
Chr7:107824700 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001037132.4(NRCAM):c.3853G>A (p.Ala1285Thr) single nucleotide variant NRCAM-related condition [RCV003895433]|not provided [RCV000886652] Chr7:108149972 [GRCh38]
Chr7:107790417 [GRCh37]
Chr7:7q31.1		 benign
NM_001037132.4(NRCAM):c.3744A>G (p.Lys1248=) single nucleotide variant not provided [RCV000975163] Chr7:108150081 [GRCh38]
Chr7:107790526 [GRCh37]
Chr7:7q31.1		 benign
NM_001037132.4(NRCAM):c.3606A>G (p.Glu1202=) single nucleotide variant not provided [RCV000910893] Chr7:108159534 [GRCh38]
Chr7:107799979 [GRCh37]
Chr7:7q31.1		 likely benign
GRCh37/hg19 7q31.1(chr7:107441501-108433812)x1 copy number loss not provided [RCV001005992] Chr7:107441501..108433812 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q22.3-31.32(chr7:106617406-123217914)x1 copy number loss not provided [RCV001005991] Chr7:106617406..123217914 [GRCh37]
Chr7:7q22.3-31.32		 pathogenic
GRCh37/hg19 7q31.1(chr7:108094786-108494963)x3 copy number gain not provided [RCV001005993] Chr7:108094786..108494963 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001037132.4(NRCAM):c.1484G>A (p.Ser495Asn) single nucleotide variant NRCAM-related condition [RCV003972101] Chr7:108194408 [GRCh38]
Chr7:107834852 [GRCh37]
Chr7:7q31.1		 benign
GRCh37/hg19 7q31.1(chr7:108025055-108085810)x1 copy number loss not provided [RCV001258817] Chr7:108025055..108085810 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2531-15C>T single nucleotide variant not provided [RCV001665822] Chr7:108181952 [GRCh38]
Chr7:107822396 [GRCh37]
Chr7:7q31.1		 benign
NM_001037132.4(NRCAM):c.1602G>A (p.Ala534=) single nucleotide variant not provided [RCV001693354] Chr7:108194290 [GRCh38]
Chr7:107834734 [GRCh37]
Chr7:7q31.1		 benign
NM_001037132.4(NRCAM):c.1631-9A>G single nucleotide variant not provided [RCV001686300] Chr7:108194180 [GRCh38]
Chr7:107834624 [GRCh37]
Chr7:7q31.1		 benign
NM_001037132.4(NRCAM):c.1633C>G (p.Pro545Ala) single nucleotide variant not provided [RCV001655151] Chr7:108194169 [GRCh38]
Chr7:107834613 [GRCh37]
Chr7:7q31.1		 benign
NM_001037132.4(NRCAM):c.2647-2A>G single nucleotide variant NRCAM-related disorder [RCV001824183] Chr7:108180429 [GRCh38]
Chr7:107820873 [GRCh37]
Chr7:7q31.1		 pathogenic
NM_001037132.4(NRCAM):c.164A>G (p.Asp55Gly) single nucleotide variant NRCAM-related disorder [RCV001824186] Chr7:108234649 [GRCh38]
Chr7:107875093 [GRCh37]
Chr7:7q31.1		 pathogenic
NM_001037132.4(NRCAM):c.2557C>T (p.Arg853Cys) single nucleotide variant Inborn genetic diseases [RCV003163938]|NRCAM-related disorder [RCV001824188] Chr7:108181911 [GRCh38]
Chr7:107822355 [GRCh37]
Chr7:7q31.1		 pathogenic|uncertain significance
NM_001037132.4(NRCAM):c.331G>T (p.Glu111Ter) single nucleotide variant NRCAM-related disorder [RCV001824185]|Neurodevelopmental disorder with neuromuscular and skeletal abnormalities [RCV002246518] Chr7:108232422 [GRCh38]
Chr7:107872866 [GRCh37]
Chr7:7q31.1		 pathogenic
NM_001037132.4(NRCAM):c.590G>A (p.Gly197Asp) single nucleotide variant NRCAM-related disorder [RCV001824192]|Neurodevelopmental disorder with neuromuscular and skeletal abnormalities [RCV002246521] Chr7:108226339 [GRCh38]
Chr7:107866783 [GRCh37]
Chr7:7q31.1		 pathogenic
NM_001037132.4(NRCAM):c.2738G>A (p.Gly913Asp) single nucleotide variant NRCAM-related disorder [RCV001824191]|Neurodevelopmental disorder with neuromuscular and skeletal abnormalities [RCV002246520] Chr7:108180336 [GRCh38]
Chr7:107820780 [GRCh37]
Chr7:7q31.1		 pathogenic
NM_001037132.4(NRCAM):c.2785C>T (p.Arg929Ter) single nucleotide variant NRCAM-related disorder [RCV001824181]|Neurodevelopmental disorder with neuromuscular and skeletal abnormalities [RCV002246516] Chr7:108180289 [GRCh38]
Chr7:107820733 [GRCh37]
Chr7:7q31.1		 pathogenic
NM_001037132.4(NRCAM):c.400T>C (p.Ser134Pro) single nucleotide variant NRCAM-related disorder [RCV001824184]|not provided [RCV002246517] Chr7:108232353 [GRCh38]
Chr7:107872797 [GRCh37]
Chr7:7q31.1		 pathogenic|uncertain significance
NM_001037132.4(NRCAM):c.2297_2302delinsTC (p.Thr766fs) indel NRCAM-related disorder [RCV001824182] Chr7:108184243..108184248 [GRCh38]
Chr7:107824687..107824692 [GRCh37]
Chr7:7q31.1		 pathogenic
NM_001037132.4(NRCAM):c.230+824G>C single nucleotide variant NRCAM-related disorder [RCV001824187] Chr7:108233759 [GRCh38]
Chr7:107874203 [GRCh37]
Chr7:7q31.1		 likely pathogenic
NM_001037132.4(NRCAM):c.2705A>C (p.Lys902Thr) single nucleotide variant Inborn genetic diseases [RCV002541338]|NRCAM-related disorder [RCV001824189] Chr7:108180369 [GRCh38]
Chr7:107820813 [GRCh37]
Chr7:7q31.1		 pathogenic|uncertain significance
NM_001037132.4(NRCAM):c.1406A>G (p.Asn469Ser) single nucleotide variant NRCAM-related disorder [RCV001824190]|Neurodevelopmental disorder with neuromuscular and skeletal abnormalities [RCV002246519] Chr7:108195818 [GRCh38]
Chr7:107836262 [GRCh37]
Chr7:7q31.1		 pathogenic
GRCh37/hg19 7q22.1-31.1(chr7:99417471-111586308) copy number loss not specified [RCV002053711] Chr7:99417471..111586308 [GRCh37]
Chr7:7q22.1-31.1		 pathogenic
GRCh37/hg19 7q22.1-31.31(chr7:100676872-119156160) copy number loss not specified [RCV002053712] Chr7:100676872..119156160 [GRCh37]
Chr7:7q22.1-31.31		 pathogenic
GRCh37/hg19 7q22.3-32.1(chr7:106984287-128949489) copy number gain not specified [RCV002053715] Chr7:106984287..128949489 [GRCh37]
Chr7:7q22.3-32.1		 pathogenic
Single allele complex Ring chromosome 7 [RCV002280646] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1 copy number loss See cases [RCV002287832] Chr7:56604613..96692931 [GRCh37]
Chr7:7p22.3-q36.3		 uncertain significance
NM_001037132.4(NRCAM):c.2795A>G (p.Asn932Ser) single nucleotide variant Inborn genetic diseases [RCV002970428] Chr7:108180279 [GRCh38]
Chr7:107820723 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.1530G>C (p.Leu510Phe) single nucleotide variant Inborn genetic diseases [RCV002864687] Chr7:108194362 [GRCh38]
Chr7:107834806 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2125C>A (p.Leu709Met) single nucleotide variant Inborn genetic diseases [RCV002841354] Chr7:108184525 [GRCh38]
Chr7:107824969 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3350C>T (p.Ser1117Phe) single nucleotide variant Inborn genetic diseases [RCV002688821] Chr7:108167037 [GRCh38]
Chr7:107807482 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.31C>T (p.Arg11Cys) single nucleotide variant Inborn genetic diseases [RCV002754161] Chr7:108240034 [GRCh38]
Chr7:107880478 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001037132.4(NRCAM):c.36A>C (p.Leu12Phe) single nucleotide variant Inborn genetic diseases [RCV002693164] Chr7:108240029 [GRCh38]
Chr7:107880473 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.1576G>T (p.Val526Phe) single nucleotide variant Inborn genetic diseases [RCV002844466] Chr7:108194316 [GRCh38]
Chr7:107834760 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2867C>T (p.Ser956Leu) single nucleotide variant Inborn genetic diseases [RCV002845762] Chr7:108178097 [GRCh38]
Chr7:107818542 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2745G>T (p.Leu915Phe) single nucleotide variant Inborn genetic diseases [RCV002737972] Chr7:108180329 [GRCh38]
Chr7:107820773 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2902C>T (p.Leu968Phe) single nucleotide variant Inborn genetic diseases [RCV002931042] Chr7:108178062 [GRCh38]
Chr7:107818507 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.1480G>A (p.Gly494Arg) single nucleotide variant Inborn genetic diseases [RCV002698628] Chr7:108194412 [GRCh38]
Chr7:107834856 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2558G>A (p.Arg853His) single nucleotide variant Inborn genetic diseases [RCV002765302] Chr7:108181910 [GRCh38]
Chr7:107822354 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001037132.4(NRCAM):c.1312T>C (p.Tyr438His) single nucleotide variant Inborn genetic diseases [RCV002955437] Chr7:108197995 [GRCh38]
Chr7:107838439 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2645G>A (p.Arg882Gln) single nucleotide variant Inborn genetic diseases [RCV002873349] Chr7:108181823 [GRCh38]
Chr7:107822267 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2297C>T (p.Thr766Met) single nucleotide variant Inborn genetic diseases [RCV002826930] Chr7:108184248 [GRCh38]
Chr7:107824692 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.671A>T (p.His224Leu) single nucleotide variant Inborn genetic diseases [RCV002702034] Chr7:108226258 [GRCh38]
Chr7:107866702 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3716G>A (p.Arg1239Gln) single nucleotide variant Inborn genetic diseases [RCV002668329] Chr7:108150109 [GRCh38]
Chr7:107790554 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.1856A>G (p.Asn619Ser) single nucleotide variant Inborn genetic diseases [RCV002986970] Chr7:108191776 [GRCh38]
Chr7:107832220 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2177G>A (p.Ser726Asn) single nucleotide variant Inborn genetic diseases [RCV002831918] Chr7:108184473 [GRCh38]
Chr7:107824917 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2995G>A (p.Gly999Ser) single nucleotide variant Inborn genetic diseases [RCV002989416] Chr7:108176586 [GRCh38]
Chr7:107817031 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3259G>A (p.Glu1087Lys) single nucleotide variant Inborn genetic diseases [RCV003010837] Chr7:108168331 [GRCh38]
Chr7:107808776 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3767T>C (p.Val1256Ala) single nucleotide variant Inborn genetic diseases [RCV002897999] Chr7:108150058 [GRCh38]
Chr7:107790503 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3266A>C (p.Glu1089Ala) single nucleotide variant Inborn genetic diseases [RCV002878843] Chr7:108168324 [GRCh38]
Chr7:107808769 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.41C>T (p.Ala14Val) single nucleotide variant Inborn genetic diseases [RCV002941620] Chr7:108240024 [GRCh38]
Chr7:107880468 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3478C>T (p.Arg1160Trp) single nucleotide variant Inborn genetic diseases [RCV002813420] Chr7:108160481 [GRCh38]
Chr7:107800926 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2053G>A (p.Glu685Lys) single nucleotide variant Inborn genetic diseases [RCV002724011] Chr7:108184597 [GRCh38]
Chr7:107825041 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.1453A>G (p.Thr485Ala) single nucleotide variant Inborn genetic diseases [RCV002724273] Chr7:108195771 [GRCh38]
Chr7:107836215 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3353G>A (p.Arg1118Gln) single nucleotide variant Inborn genetic diseases [RCV003201820] Chr7:108167034 [GRCh38]
Chr7:107807479 [GRCh37]
Chr7:7q31.1		 uncertain significance
NC_000007.13:g.(?_104456677)_(108155935_?)del deletion not provided [RCV003107618] Chr7:104456677..108155935 [GRCh37]
Chr7:7q22.2-31.1		 pathogenic
NM_001037132.4(NRCAM):c.26_29del (p.Lys9fs) deletion Neurodevelopmental disorder with neuromuscular and skeletal abnormalities [RCV003221778] Chr7:108240036..108240039 [GRCh38]
Chr7:107880480..107880483 [GRCh37]
Chr7:7q31.1		 likely pathogenic
NM_001037132.4(NRCAM):c.1075+4T>C single nucleotide variant NRCAM-related condition [RCV003914336] Chr7:108209417 [GRCh38]
Chr7:107849861 [GRCh37]
Chr7:7q31.1		 benign
NM_001037132.4(NRCAM):c.3490A>T (p.Ile1164Phe) single nucleotide variant Inborn genetic diseases [RCV003268493] Chr7:108160469 [GRCh38]
Chr7:107800914 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3889G>A (p.Val1297Ile) single nucleotide variant Inborn genetic diseases [RCV003184151] Chr7:108149936 [GRCh38]
Chr7:107790381 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3538C>T (p.Leu1180Phe) single nucleotide variant Inborn genetic diseases [RCV003193149] Chr7:108160421 [GRCh38]
Chr7:107800866 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2561T>C (p.Val854Ala) single nucleotide variant Inborn genetic diseases [RCV003172897] Chr7:108181907 [GRCh38]
Chr7:107822351 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.313A>G (p.Ile105Val) single nucleotide variant Inborn genetic diseases [RCV003309969] Chr7:108232440 [GRCh38]
Chr7:107872884 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.1079C>T (p.Ala360Val) single nucleotide variant Inborn genetic diseases [RCV003309120] Chr7:108207656 [GRCh38]
Chr7:107848100 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.979A>C (p.Ile327Leu) single nucleotide variant Inborn genetic diseases [RCV003358619] Chr7:108209517 [GRCh38]
Chr7:107849961 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.1459G>A (p.Glu487Lys) single nucleotide variant Inborn genetic diseases [RCV003379048] Chr7:108195765 [GRCh38]
Chr7:107836209 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3782G>A (p.Gly1261Glu) single nucleotide variant Inborn genetic diseases [RCV003339955] Chr7:108150043 [GRCh38]
Chr7:107790488 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.1844C>T (p.Thr615Met) single nucleotide variant Inborn genetic diseases [RCV003262613] Chr7:108191788 [GRCh38]
Chr7:107832232 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.644A>T (p.Asp215Val) single nucleotide variant Inborn genetic diseases [RCV003300228] Chr7:108226285 [GRCh38]
Chr7:107866729 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.221C>T (p.Pro74Leu) single nucleotide variant Inborn genetic diseases [RCV003375846]|NRCAM-related condition [RCV003397022] Chr7:108234592 [GRCh38]
Chr7:107875036 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3587G>A (p.Gly1196Asp) single nucleotide variant Inborn genetic diseases [RCV003346057] Chr7:108160372 [GRCh38]
Chr7:107800817 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3784G>T (p.Val1262Phe) single nucleotide variant Inborn genetic diseases [RCV003362047] Chr7:108150041 [GRCh38]
Chr7:107790486 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2201A>T (p.Glu734Val) single nucleotide variant not provided [RCV003423748] Chr7:108184449 [GRCh38]
Chr7:107824893 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.106C>A (p.Pro36Thr) single nucleotide variant not provided [RCV003423749] Chr7:108239959 [GRCh38]
Chr7:107880403 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2609C>G (p.Pro870Arg) single nucleotide variant Inborn genetic diseases [RCV003346056] Chr7:108181859 [GRCh38]
Chr7:107822303 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3500A>G (p.Gln1167Arg) single nucleotide variant Inborn genetic diseases [RCV003366700] Chr7:108160459 [GRCh38]
Chr7:107800904 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2519C>T (p.Ser840Phe) single nucleotide variant Inborn genetic diseases [RCV003369171] Chr7:108182706 [GRCh38]
Chr7:107823150 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q31.1(chr7:107981349-110641907)x3 copy number gain not provided [RCV003484699] Chr7:107981349..110641907 [GRCh37]
Chr7:7q31.1		 uncertain significance
GRCh37/hg19 7q22.3-31.1(chr7:104536649-109624996)x1 copy number loss not provided [RCV003482977] Chr7:104536649..109624996 [GRCh37]
Chr7:7q22.3-31.1		 pathogenic
NM_001037132.4(NRCAM):c.362A>T (p.Tyr121Phe) single nucleotide variant Neurodevelopmental disorder with neuromuscular and skeletal abnormalities [RCV003493111] Chr7:108232391 [GRCh38]
Chr7:107872835 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2581T>G (p.Leu861Val) single nucleotide variant Neurodevelopmental disorder with neuromuscular and skeletal abnormalities [RCV003493112] Chr7:108181887 [GRCh38]
Chr7:107822331 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2536A>G (p.Met846Val) single nucleotide variant Neurodevelopmental disorder with neuromuscular and skeletal abnormalities [RCV003493110] Chr7:108181932 [GRCh38]
Chr7:107822376 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.638G>A (p.Arg213His) single nucleotide variant Neurodevelopmental disorder with neuromuscular and skeletal abnormalities [RCV003493109] Chr7:108226291 [GRCh38]
Chr7:107866735 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2036-8G>A single nucleotide variant NRCAM-related condition [RCV003922016] Chr7:108184622 [GRCh38]
Chr7:107825066 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001037132.4(NRCAM):c.2032A>G (p.Thr678Ala) single nucleotide variant NRCAM-related condition [RCV003966900] Chr7:108189648 [GRCh38]
Chr7:107830092 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001037132.4(NRCAM):c.2572A>G (p.Asn858Asp) single nucleotide variant NRCAM-related condition [RCV003902319] Chr7:108181896 [GRCh38]
Chr7:107822340 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001037132.4(NRCAM):c.2997C>T (p.Gly999=) single nucleotide variant NRCAM-related condition [RCV003924018] Chr7:108176584 [GRCh38]
Chr7:107817029 [GRCh37]
Chr7:7q31.1		 likely benign
NM_001037132.4(NRCAM):c.1076C>T (p.Ala359Val) single nucleotide variant Inborn genetic diseases [RCV004493449] Chr7:108207659 [GRCh38]
Chr7:107848103 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.11A>C (p.Lys4Thr) single nucleotide variant Inborn genetic diseases [RCV004493450] Chr7:108240054 [GRCh38]
Chr7:107880498 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2074G>T (p.Gly692Trp) single nucleotide variant Inborn genetic diseases [RCV004493458] Chr7:108184576 [GRCh38]
Chr7:107825020 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2701A>G (p.Lys901Glu) single nucleotide variant Inborn genetic diseases [RCV004493460] Chr7:108180373 [GRCh38]
Chr7:107820817 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2956A>G (p.Thr986Ala) single nucleotide variant Inborn genetic diseases [RCV004493464] Chr7:108178008 [GRCh38]
Chr7:107818453 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.331G>C (p.Glu111Gln) single nucleotide variant Inborn genetic diseases [RCV004493465] Chr7:108232422 [GRCh38]
Chr7:107872866 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.605T>G (p.Leu202Arg) single nucleotide variant Inborn genetic diseases [RCV004493472] Chr7:108226324 [GRCh38]
Chr7:107866768 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.1058T>C (p.Ile353Thr) single nucleotide variant Inborn genetic diseases [RCV004493448] Chr7:108209438 [GRCh38]
Chr7:107849882 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2690G>A (p.Arg897His) single nucleotide variant Inborn genetic diseases [RCV004493459] Chr7:108180384 [GRCh38]
Chr7:107820828 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3410G>T (p.Gly1137Val) single nucleotide variant Inborn genetic diseases [RCV004493467] Chr7:108166977 [GRCh38]
Chr7:107807422 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.569A>G (p.Gln190Arg) single nucleotide variant Inborn genetic diseases [RCV004493470] Chr7:108226360 [GRCh38]
Chr7:107866804 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.640G>A (p.Glu214Lys) single nucleotide variant Inborn genetic diseases [RCV004493473] Chr7:108226289 [GRCh38]
Chr7:107866733 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.2747C>T (p.Pro916Leu) single nucleotide variant Inborn genetic diseases [RCV004493461] Chr7:108180327 [GRCh38]
Chr7:107820771 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.505C>T (p.Pro169Ser) single nucleotide variant Inborn genetic diseases [RCV004493469] Chr7:108231076 [GRCh38]
Chr7:107871520 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.586C>G (p.Gln196Glu) single nucleotide variant Inborn genetic diseases [RCV004493471] Chr7:108226343 [GRCh38]
Chr7:107866787 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.1214C>T (p.Pro405Leu) single nucleotide variant Inborn genetic diseases [RCV004493451] Chr7:108198093 [GRCh38]
Chr7:107838537 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.1324C>G (p.Leu442Val) single nucleotide variant Inborn genetic diseases [RCV004493452] Chr7:108197983 [GRCh38]
Chr7:107838427 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.1477A>C (p.Lys493Gln) single nucleotide variant Inborn genetic diseases [RCV004493454] Chr7:108194415 [GRCh38]
Chr7:107834859 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.1547A>T (p.Gln516Leu) single nucleotide variant Inborn genetic diseases [RCV004493455] Chr7:108194345 [GRCh38]
Chr7:107834789 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.1605G>C (p.Lys535Asn) single nucleotide variant Inborn genetic diseases [RCV004493456] Chr7:108194287 [GRCh38]
Chr7:107834731 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.274G>A (p.Asp92Asn) single nucleotide variant Inborn genetic diseases [RCV004493462] Chr7:108232479 [GRCh38]
Chr7:107872923 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.278C>T (p.Pro93Leu) single nucleotide variant Inborn genetic diseases [RCV004493463] Chr7:108232475 [GRCh38]
Chr7:107872919 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.3693C>A (p.His1231Gln) single nucleotide variant Inborn genetic diseases [RCV004493468] Chr7:108150132 [GRCh38]
Chr7:107790577 [GRCh37]
Chr7:7q31.1		 uncertain significance
NM_001037132.4(NRCAM):c.686A>T (p.Gln229Leu) single nucleotide variant Inborn genetic diseases [RCV004493474] Chr7:108226243 [GRCh38]
Chr7:107866687 [GRCh37]
Chr7:7q31.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4411
Count of miRNA genes:961
Interacting mature miRNAs:1129
Transcripts:ENST00000351718, ENST00000379022, ENST00000379024, ENST00000379028, ENST00000413765, ENST00000415105, ENST00000417701, ENST00000418239, ENST00000419936, ENST00000425651, ENST00000442580, ENST00000445634, ENST00000456431, ENST00000465585, ENST00000489800, ENST00000522550
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
RH12783  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,844,019 - 107,844,173UniSTSGRCh37
Build 367107,631,255 - 107,631,409RGDNCBI36
Celera7102,657,292 - 102,657,446RGD
Cytogenetic Map7q31UniSTS
HuRef7102,212,317 - 102,212,471UniSTS
CRA_TCAGchr7v27107,211,201 - 107,211,355UniSTS
GeneMap99-GB4 RH Map7529.99UniSTS
D7S2242  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,788,122 - 107,788,297UniSTSGRCh37
Build 367107,575,358 - 107,575,533RGDNCBI36
Celera7102,595,124 - 102,595,299RGD
Cytogenetic Map7q31UniSTS
HuRef7102,150,419 - 102,150,594UniSTS
CRA_TCAGchr7v27107,149,307 - 107,149,482UniSTS
GeneMap99-GB4 RH Map7526.02UniSTS
Whitehead-RH Map7484.1UniSTS
Whitehead-YAC Contig Map7 UniSTS
SHGC-77931  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377108,015,170 - 108,015,503UniSTSGRCh37
Build 367107,802,406 - 107,802,739RGDNCBI36
Celera7102,828,523 - 102,828,856RGD
Cytogenetic Map7q31UniSTS
HuRef7102,383,371 - 102,383,704UniSTS
CRA_TCAGchr7v27107,382,392 - 107,382,725UniSTS
TNG Radiation Hybrid Map747477.0UniSTS
SHGC-112500  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,825,122 - 107,825,282UniSTSGRCh37
Build 367107,612,358 - 107,612,518RGDNCBI36
Celera7102,632,325 - 102,632,485RGD
Cytogenetic Map7q31UniSTS
HuRef7102,187,347 - 102,187,507UniSTS
CRA_TCAGchr7v27107,186,234 - 107,186,394UniSTS
TNG Radiation Hybrid Map747409.0UniSTS
GDB:1318176  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377108,018,567 - 108,018,673UniSTSGRCh37
Build 367107,805,803 - 107,805,909RGDNCBI36
Celera7102,831,921 - 102,832,027RGD
Cytogenetic Map7q31UniSTS
HuRef7102,386,768 - 102,386,874UniSTS
CRA_TCAGchr7v27107,385,790 - 107,385,896UniSTS
WIAF-1710  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,907,962 - 107,908,168UniSTSGRCh37
Build 367107,695,198 - 107,695,404RGDNCBI36
Celera7102,721,244 - 102,721,450RGD
Cytogenetic Map7q31UniSTS
HuRef7102,276,331 - 102,276,537UniSTS
CRA_TCAGchr7v27107,275,148 - 107,275,354UniSTS
GeneMap99-GB4 RH Map7529.99UniSTS
D7S2306  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,789,371 - 107,789,595UniSTSGRCh37
Build 367107,576,607 - 107,576,831RGDNCBI36
Celera7102,596,373 - 102,596,597RGD
Cytogenetic Map7q31UniSTS
HuRef7102,151,668 - 102,151,892UniSTS
CRA_TCAGchr7v27107,150,556 - 107,150,780UniSTS
GeneMap99-GB4 RH Map7526.02UniSTS
Whitehead-RH Map7484.1UniSTS
Whitehead-YAC Contig Map7 UniSTS
NRCAM_7843  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,787,927 - 107,788,758UniSTSGRCh37
Build 367107,575,163 - 107,575,994RGDNCBI36
Celera7102,594,929 - 102,595,760RGD
HuRef7102,150,224 - 102,151,055UniSTS
CRA_TCAGchr7v27107,149,112 - 107,149,943UniSTS
GDB:1318382  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,967,417 - 107,967,610UniSTSGRCh37
Build 367107,754,653 - 107,754,846RGDNCBI36
Celera7102,780,764 - 102,780,957RGD
Cytogenetic Map7q31UniSTS
HuRef7102,335,611 - 102,335,804UniSTS
CRA_TCAGchr7v27107,334,636 - 107,334,829UniSTS
NIB455  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,844,062 - 107,844,217UniSTSGRCh37
Build 367107,631,298 - 107,631,453RGDNCBI36
Celera7102,657,335 - 102,657,490RGD
Cytogenetic Map7q31UniSTS
HuRef7102,212,360 - 102,212,515UniSTS
CRA_TCAGchr7v27107,211,244 - 107,211,399UniSTS
GeneMap99-GB4 RH Map7528.18UniSTS
Whitehead-RH Map7485.2UniSTS
NCBI RH Map71089.7UniSTS
D7S2400  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,789,395 - 107,789,483UniSTSGRCh37
Build 367107,576,631 - 107,576,719RGDNCBI36
Celera7102,596,397 - 102,596,485RGD
Cytogenetic Map7q31UniSTS
HuRef7102,151,692 - 102,151,780UniSTS
CRA_TCAGchr7v27107,150,580 - 107,150,668UniSTS
GeneMap99-GB4 RH Map7526.02UniSTS
GDB:3755063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,952,243 - 107,952,362UniSTSGRCh37
Build 367107,739,479 - 107,739,598RGDNCBI36
Celera7102,765,586 - 102,765,705RGD
Cytogenetic Map7q31UniSTS
HuRef7102,320,466 - 102,320,585UniSTS
CRA_TCAGchr7v27107,319,458 - 107,319,577UniSTS
RH11567  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,788,176 - 107,788,404UniSTSGRCh37
Build 367107,575,412 - 107,575,640RGDNCBI36
Celera7102,595,178 - 102,595,406RGD
Cytogenetic Map7q31UniSTS
HuRef7102,150,473 - 102,150,701UniSTS
CRA_TCAGchr7v27107,149,361 - 107,149,589UniSTS
GeneMap99-GB4 RH Map7526.12UniSTS
D7S2397  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,788,176 - 107,788,289UniSTSGRCh37
Build 367107,575,412 - 107,575,525RGDNCBI36
Celera7102,595,178 - 102,595,291RGD
Cytogenetic Map7q31UniSTS
HuRef7102,150,473 - 102,150,586UniSTS
CRA_TCAGchr7v27107,149,361 - 107,149,474UniSTS
GeneMap99-GB4 RH Map7526.54UniSTS
GDB:3754628  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,807,144 - 107,807,262UniSTSGRCh37
Build 367107,594,380 - 107,594,498RGDNCBI36
Celera7102,614,431 - 102,614,549RGD
Cytogenetic Map7q31UniSTS
HuRef7102,169,455 - 102,169,573UniSTS
CRA_TCAGchr7v27107,168,248 - 107,168,366UniSTS
G19850  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,788,153 - 107,788,285UniSTSGRCh37
Build 367107,575,389 - 107,575,521RGDNCBI36
Celera7102,595,155 - 102,595,287RGD
Cytogenetic Map7q31UniSTS
HuRef7102,150,450 - 102,150,582UniSTS
CRA_TCAGchr7v27107,149,338 - 107,149,470UniSTS
A002A21  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,788,153 - 107,788,285UniSTSGRCh37
Build 367107,575,389 - 107,575,521RGDNCBI36
Celera7102,595,155 - 102,595,287RGD
Cytogenetic Map7q31UniSTS
HuRef7102,150,450 - 102,150,582UniSTS
CRA_TCAGchr7v27107,149,338 - 107,149,470UniSTS
GeneMap99-GB4 RH Map7529.99UniSTS
WI-13458  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,906,542 - 107,906,668UniSTSGRCh37
Build 367107,693,778 - 107,693,904RGDNCBI36
Celera7102,719,816 - 102,719,942RGD
Cytogenetic Map7q31UniSTS
HuRef7102,274,903 - 102,275,029UniSTS
CRA_TCAGchr7v27107,273,724 - 107,273,850UniSTS
GeneMap99-GB4 RH Map7526.02UniSTS
Whitehead-RH Map7484.1UniSTS
D7S2708  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,964,271 - 107,964,475UniSTSGRCh37
Build 367107,751,507 - 107,751,711RGDNCBI36
Celera7102,777,617 - 102,777,821RGD
Cytogenetic Map7q31UniSTS
HuRef7102,332,464 - 102,332,668UniSTS
CRA_TCAGchr7v27107,331,489 - 107,331,693UniSTS
TNG Radiation Hybrid Map747452.0UniSTS
Stanford-G3 RH Map75298.0UniSTS
NCBI RH Map71086.8UniSTS
D7S2147E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,789,756 - 107,789,868UniSTSGRCh37
Build 367107,576,992 - 107,577,104RGDNCBI36
Celera7102,596,758 - 102,596,870RGD
Cytogenetic Map7q31UniSTS
HuRef7102,152,053 - 102,152,165UniSTS
CRA_TCAGchr7v27107,150,941 - 107,151,053UniSTS
TNG Radiation Hybrid Map747388.0UniSTS
Stanford-G3 RH Map75278.0UniSTS
NCBI RH Map71089.0UniSTS
GeneMap99-G3 RH Map75278.0UniSTS
HSC253  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377107,795,438 - 107,795,650UniSTSGRCh37
Build 367107,582,674 - 107,582,886RGDNCBI36
Celera7102,602,441 - 102,602,653RGD
Cytogenetic Map7q31UniSTS
HuRef7102,157,736 - 102,157,952UniSTS
CRA_TCAGchr7v27107,156,624 - 107,156,836UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component
High
Medium 33 3 608 25 172 28 650 16 3344 144 171 204 176 426 2
Low 2079 865 781 235 706 112 2088 917 347 252 1044 1320 130 856 949
Below cutoff 288 2076 310 339 952 301 1608 1247 26 19 222 70 42 1 172 1411 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_029898 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001037132 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001193582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001193583 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001193584 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371119 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371122 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371123 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371124 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371125 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371126 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371127 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371128 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371129 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371130 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371131 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371132 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371133 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371134 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371135 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371136 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371137 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371138 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371139 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371141 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371142 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371143 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371144 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371145 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371146 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371147 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371148 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371149 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371150 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371151 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371152 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371153 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371154 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371155 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371156 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371157 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371158 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371159 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371160 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371162 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371163 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371164 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371165 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371166 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371167 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371168 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371169 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371170 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371171 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371172 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371173 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371174 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371175 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371176 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371177 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371178 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371179 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371180 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371181 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371182 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_005010 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163867 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163868 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163869 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163870 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163871 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716003 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716007 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716012 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716014 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516253 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516255 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516257 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516258 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516262 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516265 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012238 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012239 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012247 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012251 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446773 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446775 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446777 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446778 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446779 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446780 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420417 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420418 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420419 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420420 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420421 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420422 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420423 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420424 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420425 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358275 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358278 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358281 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358282 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358288 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358293 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358294 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358297 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358298 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358299 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358300 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358301 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358302 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358303 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358304 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358305 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358306 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB002341 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005058 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005683 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC007567 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF172277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI031622 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ001054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ001057 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK092330 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK127035 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294195 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299870 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY528240 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC098401 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC114570 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC115736 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU735065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX538010 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX954399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH236947 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA292156 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA398450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510970 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KX533482 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KX545273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KX545274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U55258 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000351718   ⟹   ENSP00000325269
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,147,662 - 108,456,339 (-)Ensembl
RefSeq Acc Id: ENST00000379022   ⟹   ENSP00000368308
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,149,910 - 108,240,049 (-)Ensembl
RefSeq Acc Id: ENST00000379024   ⟹   ENSP00000368310
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,148,117 - 108,456,321 (-)Ensembl
RefSeq Acc Id: ENST00000379028   ⟹   ENSP00000368314
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,147,649 - 108,456,436 (-)Ensembl
RefSeq Acc Id: ENST00000413765   ⟹   ENSP00000407858
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,147,626 - 108,456,397 (-)Ensembl
RefSeq Acc Id: ENST00000415105
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,150,049 - 108,176,773 (-)Ensembl
RefSeq Acc Id: ENST00000417701   ⟹   ENSP00000390421
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,197,995 - 108,243,240 (-)Ensembl
RefSeq Acc Id: ENST00000418239   ⟹   ENSP00000393663
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,234,630 - 108,456,717 (-)Ensembl
RefSeq Acc Id: ENST00000419936   ⟹   ENSP00000397544
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,232,417 - 108,313,295 (-)Ensembl
RefSeq Acc Id: ENST00000442580   ⟹   ENSP00000390868
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,232,399 - 108,328,488 (-)Ensembl
RefSeq Acc Id: ENST00000445634   ⟹   ENSP00000398174
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,149,952 - 108,175,357 (-)Ensembl
RefSeq Acc Id: ENST00000456431   ⟹   ENSP00000408203
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,232,417 - 108,328,655 (-)Ensembl
RefSeq Acc Id: ENST00000465585
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,156,387 - 108,178,114 (-)Ensembl
RefSeq Acc Id: ENST00000489800
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,207,228 - 108,209,603 (-)Ensembl
RefSeq Acc Id: ENST00000522550
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,147,623 - 108,156,637 (-)Ensembl
RefSeq Acc Id: ENST00000613830   ⟹   ENSP00000484840
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7108,178,150 - 108,456,385 (-)Ensembl
RefSeq Acc Id: NM_001037132   ⟹   NP_001032209
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
GRCh377107,788,071 - 108,096,841 (-)NCBI
Build 367107,575,318 - 107,884,062 (-)NCBI Archive
HuRef7102,150,368 - 102,465,060 (-)ENTREZGENE
CHM1_17107,721,788 - 107,813,876 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
CRA_TCAGchr7v27107,149,256 - 107,464,062 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001193582   ⟹   NP_001180511
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
GRCh377107,788,071 - 108,096,841 (-)NCBI
HuRef7102,150,368 - 102,465,060 (-)ENTREZGENE
CHM1_17107,721,788 - 108,030,155 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
CRA_TCAGchr7v27107,149,256 - 107,464,062 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001193583   ⟹   NP_001180512
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
GRCh377107,788,071 - 108,096,841 (-)NCBI
HuRef7102,150,368 - 102,465,060 (-)ENTREZGENE
CHM1_17107,721,788 - 108,030,155 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
CRA_TCAGchr7v27107,149,256 - 107,464,062 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001193584   ⟹   NP_001180513
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
GRCh377107,788,071 - 108,096,841 (-)NCBI
HuRef7102,150,368 - 102,465,060 (-)ENTREZGENE
CHM1_17107,721,788 - 108,030,155 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
CRA_TCAGchr7v27107,149,256 - 107,464,062 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001371119   ⟹   NP_001358048
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,720 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,370 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371122   ⟹   NP_001358051
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,720 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,370 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371123   ⟹   NP_001358052
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,720 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,370 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371124   ⟹   NP_001358053
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,720 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,370 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371125   ⟹   NP_001358054
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371126   ⟹   NP_001358055
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371127   ⟹   NP_001358056
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371128   ⟹   NP_001358057
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371129   ⟹   NP_001358058
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371130   ⟹   NP_001358059
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371131   ⟹   NP_001358060
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371132   ⟹   NP_001358061
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371133   ⟹   NP_001358062
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371134   ⟹   NP_001358063
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371135   ⟹   NP_001358064
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371136   ⟹   NP_001358065
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371137   ⟹   NP_001358066
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371138   ⟹   NP_001358067
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371139   ⟹   NP_001358068
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371140   ⟹   NP_001358069
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371141   ⟹   NP_001358070
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371142   ⟹   NP_001358071
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371143   ⟹   NP_001358072
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371144   ⟹   NP_001358073
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371145   ⟹   NP_001358074
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371146   ⟹   NP_001358075
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371147   ⟹   NP_001358076
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371148   ⟹   NP_001358077
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371149   ⟹   NP_001358078
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371150   ⟹   NP_001358079
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371151   ⟹   NP_001358080
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371152   ⟹   NP_001358081
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371153   ⟹   NP_001358082
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371154   ⟹   NP_001358083
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371155   ⟹   NP_001358084
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371156   ⟹   NP_001358085
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371157   ⟹   NP_001358086
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371158   ⟹   NP_001358087
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371159   ⟹   NP_001358088
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371160   ⟹   NP_001358089
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371161   ⟹   NP_001358090
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371162   ⟹   NP_001358091
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371163   ⟹   NP_001358092
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371164   ⟹   NP_001358093
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371165   ⟹   NP_001358094
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371166   ⟹   NP_001358095
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371167   ⟹   NP_001358096
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371168   ⟹   NP_001358097
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371169   ⟹   NP_001358098
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371170   ⟹   NP_001358099
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371171   ⟹   NP_001358100
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371172   ⟹   NP_001358101
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371173   ⟹   NP_001358102
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371174   ⟹   NP_001358103
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371175   ⟹   NP_001358104
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371176   ⟹   NP_001358105
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,328,526 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,653,179 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371177   ⟹   NP_001358106
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,328,526 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,653,179 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371178   ⟹   NP_001358107
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,328,526 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,653,179 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371179   ⟹   NP_001358108
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,328,526 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,653,179 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371180   ⟹   NP_001358109
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,328,526 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,653,179 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371181   ⟹   NP_001358110
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,243,385 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,567,982 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371182   ⟹   NP_001358111
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,243,385 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,567,982 (-)NCBI
Sequence:
RefSeq Acc Id: NM_005010   ⟹   NP_005001
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
GRCh377107,788,071 - 108,096,841 (-)NCBI
Build 367107,575,318 - 107,884,062 (-)NCBI Archive
HuRef7102,150,368 - 102,465,060 (-)ENTREZGENE
CHM1_17107,721,788 - 108,030,155 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
CRA_TCAGchr7v27107,149,256 - 107,464,062 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: NR_163867
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163868
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163869
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163870
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163871
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006716003   ⟹   XP_006716066
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006716012   ⟹   XP_006716075
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006716014   ⟹   XP_006716077
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516253   ⟹   XP_011514555
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516255   ⟹   XP_011514557
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,328,526 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516257   ⟹   XP_011514559
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516258   ⟹   XP_011514560
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,328,526 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516259   ⟹   XP_011514561
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516261   ⟹   XP_011514563
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516262   ⟹   XP_011514564
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516265   ⟹   XP_011514567
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,150,695 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516267   ⟹   XP_011514569
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516268   ⟹   XP_011514570
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516269   ⟹   XP_011514571
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516270   ⟹   XP_011514572
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012236   ⟹   XP_016867725
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012238   ⟹   XP_016867727
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012239   ⟹   XP_016867728
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012246   ⟹   XP_016867735
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012247   ⟹   XP_016867736
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012248   ⟹   XP_016867737
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017012251   ⟹   XP_016867740
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024446777   ⟹   XP_024302545
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024446778   ⟹   XP_024302546
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024446779   ⟹   XP_024302547
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024446780   ⟹   XP_024302548
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,150,695 - 108,456,436 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047420417   ⟹   XP_047276373
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
RefSeq Acc Id: XM_047420418   ⟹   XP_047276374
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
RefSeq Acc Id: XM_047420419   ⟹   XP_047276375
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
RefSeq Acc Id: XM_047420420   ⟹   XP_047276376
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
RefSeq Acc Id: XM_047420421   ⟹   XP_047276377
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
RefSeq Acc Id: XM_047420422   ⟹   XP_047276378
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
RefSeq Acc Id: XM_047420423   ⟹   XP_047276379
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
RefSeq Acc Id: XM_047420424   ⟹   XP_047276380
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
RefSeq Acc Id: XM_047420425   ⟹   XP_047276381
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,147,649 - 108,456,436 (-)NCBI
RefSeq Acc Id: XM_054358272   ⟹   XP_054214247
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358273   ⟹   XP_054214248
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,653,179 (-)NCBI
RefSeq Acc Id: XM_054358274   ⟹   XP_054214249
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358275   ⟹   XP_054214250
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358276   ⟹   XP_054214251
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,653,179 (-)NCBI
RefSeq Acc Id: XM_054358277   ⟹   XP_054214252
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358278   ⟹   XP_054214253
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358279   ⟹   XP_054214254
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358280   ⟹   XP_054214255
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358281   ⟹   XP_054214256
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358282   ⟹   XP_054214257
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358283   ⟹   XP_054214258
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358284   ⟹   XP_054214259
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358285   ⟹   XP_054214260
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,468,839 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358286   ⟹   XP_054214261
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358287   ⟹   XP_054214262
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358288   ⟹   XP_054214263
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358289   ⟹   XP_054214264
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358290   ⟹   XP_054214265
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358291   ⟹   XP_054214266
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358292   ⟹   XP_054214267
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358293   ⟹   XP_054214268
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358294   ⟹   XP_054214269
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358295   ⟹   XP_054214270
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358296   ⟹   XP_054214271
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358297   ⟹   XP_054214272
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358298   ⟹   XP_054214273
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358299   ⟹   XP_054214274
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358300   ⟹   XP_054214275
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358301   ⟹   XP_054214276
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358302   ⟹   XP_054214277
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358303   ⟹   XP_054214278
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358304   ⟹   XP_054214279
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358305   ⟹   XP_054214280
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,465,793 - 109,781,086 (-)NCBI
RefSeq Acc Id: XM_054358306   ⟹   XP_054214281
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07109,468,839 - 109,781,086 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001032209 (Get FASTA)   NCBI Sequence Viewer  
  NP_001180511 (Get FASTA)   NCBI Sequence Viewer  
  NP_001180512 (Get FASTA)   NCBI Sequence Viewer  
  NP_001180513 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358048 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358051 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358052 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358053 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358054 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358055 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358056 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358057 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358058 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358059 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358060 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358061 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358062 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358063 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358064 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358065 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358066 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358067 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358068 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358069 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358070 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358071 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358072 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358073 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358074 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358075 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358076 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358077 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358078 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358079 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358080 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358081 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358082 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358083 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358084 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358085 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358086 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358087 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358088 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358089 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358090 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358091 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358092 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358093 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358094 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358095 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358096 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358097 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358098 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358099 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358100 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358101 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358102 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358103 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358104 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358105 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358106 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358107 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358108 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358109 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358110 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358111 (Get FASTA)   NCBI Sequence Viewer  
  NP_005001 (Get FASTA)   NCBI Sequence Viewer  
  XP_006716066 (Get FASTA)   NCBI Sequence Viewer  
  XP_006716075 (Get FASTA)   NCBI Sequence Viewer  
  XP_006716077 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514555 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514557 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514559 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514560 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514561 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514563 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514564 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514567 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514569 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514570 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514571 (Get FASTA)   NCBI Sequence Viewer  
  XP_011514572 (Get FASTA)   NCBI Sequence Viewer  
  XP_016867725 (Get FASTA)   NCBI Sequence Viewer  
  XP_016867727 (Get FASTA)   NCBI Sequence Viewer  
  XP_016867728 (Get FASTA)   NCBI Sequence Viewer  
  XP_016867735 (Get FASTA)   NCBI Sequence Viewer  
  XP_016867736 (Get FASTA)   NCBI Sequence Viewer  
  XP_016867737 (Get FASTA)   NCBI Sequence Viewer  
  XP_016867740 (Get FASTA)   NCBI Sequence Viewer  
  XP_024302545 (Get FASTA)   NCBI Sequence Viewer  
  XP_024302546 (Get FASTA)   NCBI Sequence Viewer  
  XP_024302547 (Get FASTA)   NCBI Sequence Viewer  
  XP_024302548 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276373 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276374 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276375 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276376 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276377 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276378 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276379 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276380 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276381 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214247 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214248 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214249 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214250 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214251 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214252 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214253 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214254 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214255 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214256 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214257 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214258 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214259 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214260 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214261 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214262 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214263 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214264 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214265 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214266 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214267 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214268 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214269 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214270 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214271 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214272 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214273 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214274 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214275 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214276 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214277 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214278 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214279 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214280 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214281 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC50765 (Get FASTA)   NCBI Sequence Viewer  
  AAF22282 (Get FASTA)   NCBI Sequence Viewer  
  AAF22283 (Get FASTA)   NCBI Sequence Viewer  
  AAH98401 (Get FASTA)   NCBI Sequence Viewer  
  AAI14571 (Get FASTA)   NCBI Sequence Viewer  
  AAI15737 (Get FASTA)   NCBI Sequence Viewer  
  AAS07434 (Get FASTA)   NCBI Sequence Viewer  
  AAS48507 (Get FASTA)   NCBI Sequence Viewer  
  ANT47184 (Get FASTA)   NCBI Sequence Viewer  
  ANT47185 (Get FASTA)   NCBI Sequence Viewer  
  AQN67635 (Get FASTA)   NCBI Sequence Viewer  
  BAA20801 (Get FASTA)   NCBI Sequence Viewer  
  BAG52532 (Get FASTA)   NCBI Sequence Viewer  
  BAG57510 (Get FASTA)   NCBI Sequence Viewer  
  BAH13156 (Get FASTA)   NCBI Sequence Viewer  
  CAA04504 (Get FASTA)   NCBI Sequence Viewer  
  CAA04507 (Get FASTA)   NCBI Sequence Viewer  
  CAD97960 (Get FASTA)   NCBI Sequence Viewer  
  EAL24386 (Get FASTA)   NCBI Sequence Viewer  
  EAW83427 (Get FASTA)   NCBI Sequence Viewer  
  EAW83428 (Get FASTA)   NCBI Sequence Viewer  
  EAW83429 (Get FASTA)   NCBI Sequence Viewer  
  EAW83430 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000325269
  ENSP00000325269.6
  ENSP00000368310
  ENSP00000368310.4
  ENSP00000368314
  ENSP00000368314.3
  ENSP00000390421.1
  ENSP00000390868.1
  ENSP00000393663.1
  ENSP00000397544.1
  ENSP00000398174.2
  ENSP00000407858
  ENSP00000407858.3
  ENSP00000408203.1
GenBank Protein Q92823 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_005001   ⟸   NM_005010
- Peptide Label: isoform B precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001180513   ⟸   NM_001193584
- Peptide Label: isoform F precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001180512   ⟸   NM_001193583
- Peptide Label: isoform E precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001180511   ⟸   NM_001193582
- Peptide Label: isoform D precursor
- UniProtKB: C9JYY6 (UniProtKB/TrEMBL),   Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001032209   ⟸   NM_001037132
- Peptide Label: isoform A precursor
- UniProtKB: Q9UHI3 (UniProtKB/Swiss-Prot),   Q14BM2 (UniProtKB/Swiss-Prot),   O15179 (UniProtKB/Swiss-Prot),   O15051 (UniProtKB/Swiss-Prot),   E9PDA4 (UniProtKB/Swiss-Prot),   A4D0S3 (UniProtKB/Swiss-Prot),   Q9UHI4 (UniProtKB/Swiss-Prot),   Q92823 (UniProtKB/Swiss-Prot),   Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006716077   ⟸   XM_006716014
- Peptide Label: isoform X18
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006716075   ⟸   XM_006716012
- Peptide Label: isoform X14
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006716066   ⟸   XM_006716003
- Peptide Label: isoform X2
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514563   ⟸   XM_011516261
- Peptide Label: isoform X6
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514559   ⟸   XM_011516257
- Peptide Label: isoform X3
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514564   ⟸   XM_011516262
- Peptide Label: isoform X7
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514561   ⟸   XM_011516259
- Peptide Label: isoform X4
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514572   ⟸   XM_011516270
- Peptide Label: isoform X19
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514571   ⟸   XM_011516269
- Peptide Label: isoform X16
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514569   ⟸   XM_011516267
- Peptide Label: isoform X13
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514555   ⟸   XM_011516253
- Peptide Label: isoform X1
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514570   ⟸   XM_011516268
- Peptide Label: isoform X15
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514560   ⟸   XM_011516258
- Peptide Label: isoform X3
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514557   ⟸   XM_011516255
- Peptide Label: isoform X1
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514567   ⟸   XM_011516265
- Peptide Label: isoform X12
- UniProtKB: B7Z670 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016867728   ⟸   XM_017012239
- Peptide Label: isoform X10
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016867736   ⟸   XM_017012247
- Peptide Label: isoform X21
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016867727   ⟸   XM_017012238
- Peptide Label: isoform X8
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016867740   ⟸   XM_017012251
- Peptide Label: isoform X23
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016867735   ⟸   XM_017012246
- Peptide Label: isoform X17
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016867725   ⟸   XM_017012236
- Peptide Label: isoform X5
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016867737   ⟸   XM_017012248
- Peptide Label: isoform X22
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024302547   ⟸   XM_024446779
- Peptide Label: isoform X31
- UniProtKB: A0A1S5UZH4 (UniProtKB/TrEMBL),   Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024302546   ⟸   XM_024446778
- Peptide Label: isoform X26
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024302545   ⟸   XM_024446777
- Peptide Label: isoform X24
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024302548   ⟸   XM_024446780
- Peptide Label: isoform X33
- UniProtKB: B7Z670 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001358051   ⟸   NM_001371122
- Peptide Label: isoform E precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358053   ⟸   NM_001371124
- Peptide Label: isoform H precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358048   ⟸   NM_001371119
- Peptide Label: isoform P precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358052   ⟸   NM_001371123
- Peptide Label: isoform G precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358080   ⟸   NM_001371151
- Peptide Label: isoform B precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358093   ⟸   NM_001371164
- Peptide Label: isoform L
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358077   ⟸   NM_001371148
- Peptide Label: isoform M
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358099   ⟸   NM_001371170
- Peptide Label: isoform hh
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358054   ⟸   NM_001371125
- Peptide Label: isoform I
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358072   ⟸   NM_001371143
- Peptide Label: isoform L
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358066   ⟸   NM_001371137
- Peptide Label: isoform U
RefSeq Acc Id: NP_001358063   ⟸   NM_001371134
- Peptide Label: isoform R precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358104   ⟸   NM_001371175
- Peptide Label: isoform kk precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358086   ⟸   NM_001371157
- Peptide Label: isoform dd precursor
- UniProtKB: B7Z670 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358065   ⟸   NM_001371136
- Peptide Label: isoform T precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358081   ⟸   NM_001371152
- Peptide Label: isoform K precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358089   ⟸   NM_001371160
- Peptide Label: isoform ff precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358076   ⟸   NM_001371147
- Peptide Label: isoform I
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358071   ⟸   NM_001371142
- Peptide Label: isoform Y
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358083   ⟸   NM_001371154
- Peptide Label: isoform O precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358069   ⟸   NM_001371140
- Peptide Label: isoform W precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358075   ⟸   NM_001371146
- Peptide Label: isoform aa precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358058   ⟸   NM_001371129
- Peptide Label: isoform J precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358087   ⟸   NM_001371158
- Peptide Label: isoform ee precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358074   ⟸   NM_001371145
- Peptide Label: isoform Z precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358101   ⟸   NM_001371172
- Peptide Label: isoform H precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358064   ⟸   NM_001371135
- Peptide Label: isoform S precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358056   ⟸   NM_001371127
- Peptide Label: isoform Q precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358103   ⟸   NM_001371174
- Peptide Label: isoform jj precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358079   ⟸   NM_001371150
- Peptide Label: isoform bb precursor
- UniProtKB: B7Z670 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358088   ⟸   NM_001371159
- Peptide Label: isoform ll precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358090   ⟸   NM_001371161
- Peptide Label: isoform N precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358067   ⟸   NM_001371138
- Peptide Label: isoform V precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358098   ⟸   NM_001371169
- Peptide Label: isoform gg precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358102   ⟸   NM_001371173
- Peptide Label: isoform ii precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358078   ⟸   NM_001371149
- Peptide Label: isoform G precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358085   ⟸   NM_001371156
- Peptide Label: isoform cc precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358062   ⟸   NM_001371133
- Peptide Label: isoform B precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358073   ⟸   NM_001371144
- Peptide Label: isoform D precursor
- UniProtKB: C9JYY6 (UniProtKB/TrEMBL),   Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358070   ⟸   NM_001371141
- Peptide Label: isoform X precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358100   ⟸   NM_001371171
- Peptide Label: isoform B precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358091   ⟸   NM_001371162
- Peptide Label: isoform F precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358068   ⟸   NM_001371139
- Peptide Label: isoform E precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358055   ⟸   NM_001371126
- Peptide Label: isoform H precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358082   ⟸   NM_001371153
- Peptide Label: isoform N precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358097   ⟸   NM_001371168
- Peptide Label: isoform D precursor
- UniProtKB: C9JYY6 (UniProtKB/TrEMBL),   Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358092   ⟸   NM_001371163
- Peptide Label: isoform E precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358060   ⟸   NM_001371131
- Peptide Label: isoform A precursor
- UniProtKB: Q9UHI3 (UniProtKB/Swiss-Prot),   Q92823 (UniProtKB/Swiss-Prot),   Q14BM2 (UniProtKB/Swiss-Prot),   O15179 (UniProtKB/Swiss-Prot),   O15051 (UniProtKB/Swiss-Prot),   E9PDA4 (UniProtKB/Swiss-Prot),   A4D0S3 (UniProtKB/Swiss-Prot),   Q9UHI4 (UniProtKB/Swiss-Prot),   Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358059   ⟸   NM_001371130
- Peptide Label: isoform K precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358094   ⟸   NM_001371165
- Peptide Label: isoform E precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358084   ⟸   NM_001371155
- Peptide Label: isoform E precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358095   ⟸   NM_001371166
- Peptide Label: isoform O precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358061   ⟸   NM_001371132
- Peptide Label: isoform J precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358096   ⟸   NM_001371167
- Peptide Label: isoform E precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358057   ⟸   NM_001371128
- Peptide Label: isoform D precursor
- UniProtKB: C9JYY6 (UniProtKB/TrEMBL),   Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358109   ⟸   NM_001371180
- Peptide Label: isoform M
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358107   ⟸   NM_001371178
- Peptide Label: isoform B precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358105   ⟸   NM_001371176
- Peptide Label: isoform K precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358108   ⟸   NM_001371179
- Peptide Label: isoform M
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358106   ⟸   NM_001371177
- Peptide Label: isoform E precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358111   ⟸   NM_001371182
- Peptide Label: isoform mm precursor
- UniProtKB: A0A1S5UZH4 (UniProtKB/TrEMBL),   Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001358110   ⟸   NM_001371181
- Peptide Label: isoform E precursor
- UniProtKB: Q14CA1 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000407858   ⟸   ENST00000413765
RefSeq Acc Id: ENSP00000484840   ⟸   ENST00000613830
RefSeq Acc Id: ENSP00000408203   ⟸   ENST00000456431
RefSeq Acc Id: ENSP00000390868   ⟸   ENST00000442580
RefSeq Acc Id: ENSP00000390421   ⟸   ENST00000417701
RefSeq Acc Id: ENSP00000393663   ⟸   ENST00000418239
RefSeq Acc Id: ENSP00000368314   ⟸   ENST00000379028
RefSeq Acc Id: ENSP00000368308   ⟸   ENST00000379022
RefSeq Acc Id: ENSP00000368310   ⟸   ENST00000379024
RefSeq Acc Id: ENSP00000325269   ⟸   ENST00000351718
RefSeq Acc Id: ENSP00000397544   ⟸   ENST00000419936
RefSeq Acc Id: ENSP00000398174   ⟸   ENST00000445634
RefSeq Acc Id: XP_047276381   ⟸   XM_047420425
- Peptide Label: isoform X32
RefSeq Acc Id: XP_047276378   ⟸   XM_047420422
- Peptide Label: isoform X28
RefSeq Acc Id: XP_047276380   ⟸   XM_047420424
- Peptide Label: isoform X30
RefSeq Acc Id: XP_047276373   ⟸   XM_047420417
- Peptide Label: isoform X9
RefSeq Acc Id: XP_047276379   ⟸   XM_047420423
- Peptide Label: isoform X29
RefSeq Acc Id: XP_047276377   ⟸   XM_047420421
- Peptide Label: isoform X27
RefSeq Acc Id: XP_047276374   ⟸   XM_047420418
- Peptide Label: isoform X11
RefSeq Acc Id: XP_047276376   ⟸   XM_047420420
- Peptide Label: isoform X25
RefSeq Acc Id: XP_047276375   ⟸   XM_047420419
- Peptide Label: isoform X20
RefSeq Acc Id: XP_054214263   ⟸   XM_054358288
- Peptide Label: isoform X15
RefSeq Acc Id: XP_054214280   ⟸   XM_054358305
- Peptide Label: isoform X32
RefSeq Acc Id: XP_054214276   ⟸   XM_054358301
- Peptide Label: isoform X28
RefSeq Acc Id: XP_054214279   ⟸   XM_054358304
- Peptide Label: isoform X31
RefSeq Acc Id: XP_054214278   ⟸   XM_054358303
- Peptide Label: isoform X30
RefSeq Acc Id: XP_054214258   ⟸   XM_054358283
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054214274   ⟸   XM_054358299
- Peptide Label: isoform X26
RefSeq Acc Id: XP_054214257   ⟸   XM_054358282
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054214254   ⟸   XM_054358279
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054214272   ⟸   XM_054358297
- Peptide Label: isoform X24
RefSeq Acc Id: XP_054214250   ⟸   XM_054358275
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054214277   ⟸   XM_054358302
- Peptide Label: isoform X29
RefSeq Acc Id: XP_054214275   ⟸   XM_054358300
- Peptide Label: isoform X27
RefSeq Acc Id: XP_054214259   ⟸   XM_054358284
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054214269   ⟸   XM_054358294
- Peptide Label: isoform X21
RefSeq Acc Id: XP_054214273   ⟸   XM_054358298
- Peptide Label: isoform X25
RefSeq Acc Id: XP_054214256   ⟸   XM_054358281
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054214255   ⟸   XM_054358280
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054214271   ⟸   XM_054358296
- Peptide Label: isoform X23
RefSeq Acc Id: XP_054214268   ⟸   XM_054358293
- Peptide Label: isoform X20
RefSeq Acc Id: XP_054214265   ⟸   XM_054358290
- Peptide Label: isoform X17
RefSeq Acc Id: XP_054214253   ⟸   XM_054358278
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054214270   ⟸   XM_054358295
- Peptide Label: isoform X22
RefSeq Acc Id: XP_054214252   ⟸   XM_054358277
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054214266   ⟸   XM_054358291
- Peptide Label: isoform X18
RefSeq Acc Id: XP_054214262   ⟸   XM_054358287
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054214249   ⟸   XM_054358274
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054214267   ⟸   XM_054358292
- Peptide Label: isoform X19
RefSeq Acc Id: XP_054214264   ⟸   XM_054358289
- Peptide Label: isoform X16
RefSeq Acc Id: XP_054214261   ⟸   XM_054358286
- Peptide Label: isoform X13
RefSeq Acc Id: XP_054214247   ⟸   XM_054358272
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054214251   ⟸   XM_054358276
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054214248   ⟸   XM_054358273
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054214281   ⟸   XM_054358306
- Peptide Label: isoform X33
RefSeq Acc Id: XP_054214260   ⟸   XM_054358285
- Peptide Label: isoform X12
Protein Domains
Fibronectin type-III   Ig-like   Neurofascin/L1/NrCAM C-terminal

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q92823-F1-model_v2 AlphaFold Q92823 1-1304 view protein structure

Promoters
RGD ID:6805965
Promoter ID:HG_KWN:59266
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell
Transcripts:ENST00000379022,   ENST00000379024,   ENST00000379028,   ENST00000379032,   NM_001037132,   NM_005010,   OTTHUMT00000337938,   OTTHUMT00000338039,   UC003VFD.1,   UC003VFE.1
Position:
Human AssemblyChrPosition (strand)Source
Build 367107,883,711 - 107,884,211 (-)MPROMDB
RGD ID:7211651
Promoter ID:EPDNEW_H11571
Type:single initiation site
Name:NRCAM_1
Description:neuronal cell adhesion molecule
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11573  EPDNEW_H11572  EPDNEW_H11574  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,262,121 - 108,262,181EPDNEW
RGD ID:7211655
Promoter ID:EPDNEW_H11572
Type:initiation region
Name:NRCAM_3
Description:neuronal cell adhesion molecule
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11571  EPDNEW_H11573  EPDNEW_H11574  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,456,234 - 108,456,294EPDNEW
RGD ID:7211653
Promoter ID:EPDNEW_H11573
Type:initiation region
Name:NRCAM_2
Description:neuronal cell adhesion molecule
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11571  EPDNEW_H11572  EPDNEW_H11574  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,456,385 - 108,456,445EPDNEW
RGD ID:7211657
Promoter ID:EPDNEW_H11574
Type:initiation region
Name:NRCAM_4
Description:neuronal cell adhesion molecule
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11571  EPDNEW_H11573  EPDNEW_H11572  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387108,456,720 - 108,456,780EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:7994 AgrOrtholog
COSMIC NRCAM COSMIC
Ensembl Genes ENSG00000091129 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000351718 ENTREZGENE
  ENST00000351718.8 UniProtKB/Swiss-Prot
  ENST00000379024 ENTREZGENE
  ENST00000379024.8 UniProtKB/Swiss-Prot
  ENST00000379028 ENTREZGENE
  ENST00000379028.8 UniProtKB/Swiss-Prot
  ENST00000413765 ENTREZGENE
  ENST00000413765.6 UniProtKB/TrEMBL
  ENST00000417701.5 UniProtKB/TrEMBL
  ENST00000418239.1 UniProtKB/TrEMBL
  ENST00000419936.5 UniProtKB/TrEMBL
  ENST00000442580.5 UniProtKB/TrEMBL
  ENST00000445634.2 UniProtKB/TrEMBL
  ENST00000456431.5 UniProtKB/TrEMBL
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000091129 GTEx
HGNC ID HGNC:7994 ENTREZGENE
Human Proteome Map NRCAM Human Proteome Map
InterPro FN3_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FN3_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig/MHC_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_I-set UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_sub UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_sub2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Neurofascin/L1/NrCAM_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:4897 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 4897 ENTREZGENE
OMIM 601581 OMIM
PANTHER NEURONAL CELL ADHESION MOLECULE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN SIDEKICK UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Bravo_FIGEY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  fn3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  I-set UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA31773 PharmGKB
PIRSF TyrPK_CSF1-R UniProtKB/TrEMBL
PROSITE FN3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  IG_LIKE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  IG_MHC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART FN3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  IGc2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00409 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48726 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF49265 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A1B1PFW4_HUMAN UniProtKB/TrEMBL
  A0A1S5UZH4 ENTREZGENE, UniProtKB/TrEMBL
  A4D0S3 ENTREZGENE
  B7Z670 ENTREZGENE, UniProtKB/TrEMBL
  C9J8B6_HUMAN UniProtKB/TrEMBL
  C9JF43_HUMAN UniProtKB/TrEMBL
  C9JH43_HUMAN UniProtKB/TrEMBL
  C9JUR7_HUMAN UniProtKB/TrEMBL
  C9JYY6 ENTREZGENE, UniProtKB/TrEMBL
  E9PDA4 ENTREZGENE
  H7C132_HUMAN UniProtKB/TrEMBL
  NRCAM_HUMAN UniProtKB/Swiss-Prot
  O15051 ENTREZGENE
  O15179 ENTREZGENE
  Q14BM2 ENTREZGENE
  Q14CA1 ENTREZGENE, UniProtKB/TrEMBL
  Q4KMQ7_HUMAN UniProtKB/TrEMBL
  Q6QRP2_HUMAN UniProtKB/TrEMBL
  Q75ML9_HUMAN UniProtKB/TrEMBL
  Q92823 ENTREZGENE
  Q9UHI3 ENTREZGENE
  Q9UHI4 ENTREZGENE
UniProt Secondary A4D0S3 UniProtKB/Swiss-Prot
  E9PDA4 UniProtKB/Swiss-Prot
  O15051 UniProtKB/Swiss-Prot
  O15179 UniProtKB/Swiss-Prot
  Q14BM2 UniProtKB/Swiss-Prot
  Q9UHI3 UniProtKB/Swiss-Prot
  Q9UHI4 UniProtKB/Swiss-Prot