ZMP
cntnap2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens contactin associated protein [Source:UniProtKB/TrEMBL;Acc:B0S7S0]
Human Orthologues:
AL953854.2, CNTNAP1, CNTNAP3, CNTNAP3B, CNTNAP4, CNTNAP5
Human Descriptions:
Novel protein similar to contactin associated protein-like 3 (CNTNAP3) [Source:UniProtKB/TrEMBL;Acc:
contactin associated protein 1 [Source:HGNC Symbol;Acc:8011]
contactin associated protein-like 3 [Source:HGNC Symbol;Acc:13834]
contactin associated protein-like 3B [Source:HGNC Symbol;Acc:32035]
contactin associated protein-like 4 [Source:HGNC Symbol;Acc:18747]
contactin associated protein-like 5 [Source:HGNC Symbol;Acc:18748]
contactin associated protein 1 [Source:HGNC Symbol;Acc:8011]
contactin associated protein-like 3 [Source:HGNC Symbol;Acc:13834]
contactin associated protein-like 3B [Source:HGNC Symbol;Acc:32035]
contactin associated protein-like 4 [Source:HGNC Symbol;Acc:18747]
contactin associated protein-like 5 [Source:HGNC Symbol;Acc:18748]
Mouse Orthologues:
Cntnap1, Cntnap3, Cntnap4, Cntnap5a, Cntnap5b, Cntnap5c
Mouse Descriptions:
contactin associated protein-like 1 Gene [Source:MGI Symbol;Acc:MGI:1858201]
contactin associated protein-like 3 Gene [Source:MGI Symbol;Acc:MGI:3588199]
contactin associated protein-like 4 Gene [Source:MGI Symbol;Acc:MGI:2183572]
contactin associated protein-like 5A Gene [Source:MGI Symbol;Acc:MGI:3643623]
contactin associated protein-like 5B Gene [Source:MGI Symbol;Acc:MGI:3664583]
contactin associated protein-like 5C Gene [Source:MGI Symbol;Acc:MGI:3646013]
contactin associated protein-like 3 Gene [Source:MGI Symbol;Acc:MGI:3588199]
contactin associated protein-like 4 Gene [Source:MGI Symbol;Acc:MGI:2183572]
contactin associated protein-like 5A Gene [Source:MGI Symbol;Acc:MGI:3643623]
contactin associated protein-like 5B Gene [Source:MGI Symbol;Acc:MGI:3664583]
contactin associated protein-like 5C Gene [Source:MGI Symbol;Acc:MGI:3646013]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39945 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39945
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108900 | Essential Splice Site | 378 | 621 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 2 (position 50859851)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 50555383 |
GRCz11 | 2 | 50289613 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCAGCTCAAAGACACAGGACTACCTGGCCGTAGTGCTGAGACACAATG[G/A]TGAGACAACTCTGATTTAAAGCTTTGGGGATATGAGGGACACATTTATTT
Long Flanking Sequence:
ATTCTGATAAATATATTTAATTTAATAATAAAAAAAAATGTATTTGTAGTCTGTAATGTTGATTATTATCACTTAAATTCATCCTTACTGAATAAAAAAGGAAAAATGCCTAAAAATTCACATTTGAACCCTATTAATAATGCTATATATGTGCTATAAAGTTAAAATAAAGGCGTTAGATGATCTGAATCTGTGTTGTAACACATTTAAATCTTCCCTGCTTGTGTTCTCTGTGGCAGAACAGAAGTAAGCATTTGTCTCTGTTACAGATGTTGGAGGGTATTTCGAGAGTGGGACGCTGGTGCGTTTTGACCTGATGTCCGAGAGCAGCACTTCCTCTCCTGCACTAAAGGAAGGCGAGTCTGCGGTGCTGGGCATTGTGGGTAATCTGACGCACGAGGAGCTCAGCTTTAGCTTCAGCACATCCAACACGCCGGCTGTCCTCATCTACATCAGCTCAAAGACACAGGACTACCTGGCCGTAGTGCTGAGACACAATG[G/A]TGAGACAACTCTGATTTAAAGCTTTGGGGATATGAGGGACACATTTATTTTTCTTAATAATAGCCTTAGATGATGTTGTTTTTATTGACGTTGAAATGCTTTTATAAGTGGAAATTTAGTTATGTCTTGATGTGTGTGTGTTTTTGCAGTATGTTCATGTGTTCATTAGTTTAATGTTCATTAGTTTAATTTAAAAAATTTATTTGTTTAGTTATATTGGTAACACTAATGTTCTAAATAACTAAATAACTCCTCTCTAATAACTGATTTATTTTATCTTTTATCTTTATGACAGTAAATAATATTTGACTAGATATTTTTAAAGACACTTTTGTACAGCTTACAGTGACATTTAAAGGTTTAACTAGGTTAACTAGGCAAGCTAGGGTAATTGGGCAAGTTATTGTATAATGATGGTTTGTTTTGTAGACAATCGAAAAAAAAATTAACTTAAAGTTGCTGATAATTTTGTCCCAAAAATGGTGTTTTAAAAAATAAAA
Associated Phenotype:
Not determined