ZMP
si:ch211-247h9.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate contactin 4 (CNTN4) [Source:UniProtKB/TrEMBL;Acc:B8JI47]
Human Orthologues:
CNTN3, CNTN4, CNTN6
Human Descriptions:
contactin 3 (plasmacytoma associated) [Source:HGNC Symbol;Acc:2173]
contactin 4 [Source:HGNC Symbol;Acc:2174]
contactin 6 [Source:HGNC Symbol;Acc:2176]
contactin 4 [Source:HGNC Symbol;Acc:2174]
contactin 6 [Source:HGNC Symbol;Acc:2176]
Mouse Orthologues:
Cntn3, Cntn4, Cntn6
Mouse Descriptions:
contactin 3 Gene [Source:MGI Symbol;Acc:MGI:99534]
contactin 4 Gene [Source:MGI Symbol;Acc:MGI:1095737]
contactin 6 Gene [Source:MGI Symbol;Acc:MGI:1858223]
contactin 4 Gene [Source:MGI Symbol;Acc:MGI:1095737]
contactin 6 Gene [Source:MGI Symbol;Acc:MGI:1858223]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14505 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14505
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091416 | Nonsense | 538 | 1028 | 12 | 22 |
ENSDART00000131355 | Nonsense | 538 | 998 | 13 | 22 |
The following transcripts of ENSDARG00000062880 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 11948637)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 11907439 |
GRCz11 | 23 | 11842409 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCCCATGTCAGGTGTCACGTGACCCTTCACTGGATGTCAGAKTCACCTG[G/A]TTTTTCAATGAACAGCTGATYAACTTTGGAAGCCATGGGGGATATTTYGA
Long Flanking Sequence:
AAGTATATTCTAGGTCTGATTCTAGTGGGAAAGTTATCATATTGCATTGTTCGTATATATCTTAACATGTACATTGTGGTAAGAGCAAGGATTTCAAATATTGGGGGGGGGAGACAATTTAGCCATTTCAGATTTCTTGAGGTACTTGGTGTTTATAGTGGAAACAGTTGTACTTTTACAAGGCGCAATTTCTTTCTATTGATGAAAAACTAAGAGCATAGTGACATCTAGTGGTGCTAGAATTGTGCTACAACAGCACTGATTAACACGTTACCTCTTGATCTACTGATTATTTTCAAAAATGTTACCGGCGAATATCATGTCTTTCAATACAATAAATGCTGTTTTATGTATATTATAAATGCATTTTCTCTAATTGTCATTTTAGAACCAACCATCATAACATCCAAAGCCACCCAGCTGGATGTCACAGTTGGAGAGAGTGTTGTTATCCCATGTCAGGTGTCACGTGACCCTTCACTGGATGTCAGATTCACCTG[G/A]TTTTTCAATGAACAGCTGATCAACTTTGGAAGCCATGGGGGATATTTTGAAAAAGTTGGTGGTGTATGTGCAGCTCTATTATTCATTCATTTTTAGCTTGTTTGGTTTTTTTTTTTTCCTGACCAACACATGACATGACCAGTCAAAGAAATCAGGCAATCAGCTCATAACGAGCAAGAAGCTGCTTAAACAAGCAGCCATGTGTCAAAACTAGCCCATGCAGTTTTTTTAGCAAATCATAATGTAAAACATTATGATGCCCAAACTAGGGCCTGGGGGGCAAAGATGGCCCATGCTAACTTTTGATTTGGACGCCACCCCATCTATGAATGGATTATGTATATATTATCATTTCAAATGTAATGTAAAATTTTATTTGTTTGTTTTTTTTTTGCTACAAAAAAGCTATTTGAAATTAAATGCTTTAATTTAAATGCTGTCAATTAATCAGATATATATATATATATATTATTATTACTGTTATTATATATAGACTTTAG
Associated Phenotype:
Not determined