KEGG T01001: 55612

Homo sapiens (human): 55612

Entry

55612 CDS T01001

Gene name

FERMT1, C20orf42, DTGCU2, KIND1, UNC112A, URP1

Definition

fermitin family member 1

Organism

hsa Homo sapiens (human)

Disease

H00588

Kindler syndrome

Class

SSDB

Motif

Pfam:

FERM_M FERM_N PH PH_11

Other DBs

NCBI-GI:

NCBI-GeneID:

OMIM:

HGNC:

HPRD:

Ensembl:

Vega:

UniProt:

Position

20p12.3

AA seq 677 aa
MLSSTDFTFASWELVVRVDHPNEEQQKDVTLRVSGDLHVGGVMLKLVEQINISQDWSDFA
LWWEQKHCWLLKTHWTLDKYGVQADAKLLFTPQHKMLRLRLPNLKMVRLRVSFSAVVFKA
VSDICKILNIRRSEELSLLKPSGDYFKKKKKKDKNNKEPIIEDILNLESSPTASGSSVSP
GLYSKTMTPIYDPINGTPASSTMTWFSDSPLTEQNCSILAFSQPPQSPEALADMYQPRSL
VDKAKLNAGWLDSSRSLMEQGIQEDEQLLLRFKYYSFFDLNPKYDAVRINQLYEQARWAI
LLEEIDCTEEEMLIFAALQYHISKLSLSAETQDFAGESEVDEIEAALSNLEVTLEGGKAD
SLLEDITDIPKLADNLKLFRPKKLLPKAFKQYWFIFKDTSIAYFKNKELEQGEPLEKLNL
RGCEVVPDVNVAGRKFGIKLLIPVADGMNEMYLRCDHENQYAQWMAACMLASKGKTMADS
SYQPEVLNILSFLRMKNRNSASQVASSLENMDMNPECFVSPRCAKRHKSKQLAARILEAH
QNVAQMPLVEAKLRFIQAWQSLPEFGLTYYLVRFKGSKKDDILGVSYNRLIKIDAATGIP
VTTWRFTNIKQWNVNWETRQVVIEFDQNVFTAFTCLSADCKIVHEYIGGYIFLSTRSKDQ
NETLDEDLFHKLTGGQD

NT seq 2034 nt +upstreamnt +downstreamnt
atgctgtcatccactgactttacatttgcttcctgggagcttgtggtccgcgttgaccat
cccaatgaagagcagcagaaagacgtcacactgagagtatctggagaccttcatgttgga
ggagtgatgctcaagttagtagaacagatcaatatatcccaagactggtcagactttgct
ctttggtgggaacagaagcattgctggcttctgaaaacccactggaccctggacaaatat
ggggtccaggcagatgcaaagcttctcttcacccctcagcataaaatgctgcgccttcgt
ctgccgaatttgaagatggtgaggttgcgagtcagcttctcagctgtggtttttaaagct
gtcagtgatatctgcaaaatcctgaatattagaagatcagaagagctttccttgttaaag
ccgtctggtgactattttaagaagaagaagaaaaaagacaaaaataataaggaacccata
attgaagatattctaaacctggagagttctccaacagcttcaggttcatcagtaagtcct
ggtttatacagtaaaaccatgacccctatatatgaccccatcaatggaacaccagcatca
tccaccatgacttggttcagtgacagccctttgacggaacaaaactgcagcatcctcgca
ttcagccaacccccccagtccccagaagcacttgcggatatgtaccagcctcggtctctg
gttgataaagccaagctcaatgcaggttggctagactcctcacgctcccttatggaacaa
ggcatccaagaggatgagcagctgctcttacgatttaaatattattctttcttcgacttg
aatcctaaatatgatgctgtccgaataaaccaactctatgagcaagccaggtgggccatt
ctcttagaagaaattgattgcacagaggaagaaatgttgatctttgcagctctacagtac
cacattagcaaactgtcgttgtctgctgaaacacaggattttgcaggcgagtccgaggtt
gatgaaatagaagcggcgctttctaatttggaagtaaccctagaaggtggaaaagcggac
agccttttggaggacattactgatatccctaaacttgcagataatctcaaattatttagg
cccaagaagttactaccaaaagctttcaaacaatattggtttatctttaaagacacatcc
atagcatactttaaaaataaggaacttgaacaaggagaaccactagaaaaactaaatctt
agaggctgcgaagttgtgcccgatgtaaatgtagcaggaagaaaatttggaatcaagtta
ctaatccctgttgccgatggtatgaatgaaatgtatttgagatgtgaccatgagaatcaa
tacgcccaatggatggctgcctgcatgttggcatcgaagggcaaaaccatggcagacagc
tcctaccagccagaggtcctcaacatcctttcatttctgaggatgaaaaacaggaactct
gcatctcaggtggcttccagtctcgaaaacatggatatgaacccagaatgttttgtgtca
ccacggtgtgcaaaaagacacaaatccaaacagctggccgcccggatcctggaggcgcac
cagaacgtggcccagatgcccctggtcgaagccaagctgcggttcatccaggcgtggcag
tcactgcctgagtttggcctcacctactaccttgtcagatttaaaggaagcaaaaaagat
gacattctgggagtttcatataacaggttgattaaaattgatgcagccaccgggattcca
gtgacaacatggagattcacaaatatcaaacagtggaatgtaaactgggaaacccggcag
gtggtcatcgagtttgaccaaaacgtctttactgctttcacctgcctgagtgcagattgc
aagattgtgcacgagtacattggcggctacattttcttgtccacccgctccaaggaccag
aatgaaacactcgatgaggacttgttccacaaattgaccggcggtcaggattga

All links

Ontology (1)   
   KEGG BRITE (1)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (17)   
   NCBI-Gene (1)   
   NCBI-GI (10)   
   UniGene (1)   
   HGNC (1)   
   HPRD (1)   
   ENSEMBL-HSA (1)   
   OC (1)   
   VEGA (1)   
Protein sequence (4)   
   UniProt (3)   
   RefSeq(pep) (1)   
DNA sequence (27)   
   RefSeq(nuc) (1)   
   GenBank (13)   
   EMBL (13)   
Protein domain (4)   
   Pfam (4)   
All databases (57)   

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