ZMP
si:ch211-122m3.1
Ensembl ID:
ZFIN ID:
Human Orthologues:
AL953854.2, CNTNAP3, CNTNAP3B, CNTNAP4, CNTNAP5
Human Descriptions:
Novel protein similar to contactin associated protein-like 3 (CNTNAP3) [Source:UniProtKB/TrEMBL;Acc:
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-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:
Cntnap3, Cntnap4, Cntnap5a, Cntnap5b, Cntnap5c
Mouse Descriptions:
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 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 are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa15180 | Essential Splice Site | Available for shipment | Available now |
| sa16329 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15180
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097695 | Essential Splice Site | 130 | 1300 | 3 | 24 |
| ENSDART00000136363 | Essential Splice Site | 101 | 1271 | 2 | 23 |
The following transcripts of ENSDARG00000067824 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 2281587)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 2227466 |
| GRCz11 | 10 | 2255180 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGACAYGGGACACAACTGGAGACCGTACCGCCAGGAAGACAGCATAGGG[G/T]TAAGCTTTCAATYCCCTYGGATNGAGAAAAACATGCMTTGGCCTGAKAAA
Long Flanking Sequence:
AATAAATACATAATATGAAATATATTAAAACATATTTAACAAATATTTAATAAAAGACACATACATATATTGATAAGTGGTCATATTAAATAGATGTATGTTTTATATATTTATTTTTTTACTTTATCATATTATTACAATCAAGAATACATAATAATATGTGTCATATTGACTGAATTGTTTCATGTTTAATTTATCTAAATTTGCTAAATCTAATAATTTAACTTAATTCCTTCATGTTCCAACACAAATCAATTGTGTGGATTCCGGCATTTCTTACAGTGCATGTGTGTGTGTGTCGTGCAGGTGCTGGGGGCTGGTCTCCGCTGGACTCTAATAAGTATCAGTGGCTGGAGATCAAGCTGGAGCAGCGCACTGAGATTACGGGGGTCTCCAGCCAGGGCCGATACGGCAGCTCAGACTGGGTCACTCGCTACCTCCTCATGTTCAGTGACACGGGACACAACTGGAGACCGTACCGCCAGGAAGACAGCATAGGG[G/T]TAAGCTTTCAATCCCCTCGGATGGAGAAAAACATGCATTGGCCTGATAAAACACCACATAGATTTTAGACGTTTTTAGGCCTGTGAGAAATCAACAACATCACACGAATGGTTGTTTTCCGGCGGATGTTGATGTGGTTCGGGTTTCTCCTTGAATGTGGTATCCACAATCAGATTAAAGACAAGTGGATTATATTATTTATTGTGTATTTAGTTTTTTCTGTATGTGTAAATATATACATGTACCGTGTCATATCTCTCAGCTCTTACTGTAATTTTTCTGGGGTCAATCACAGGTCATTATATATATATATATATATATATATATATATATATATATATATATATATATATATAATATAAGATGTATTAACTAGTTAAGGAGTTTTTTTCAGCACAGATCAGACATCAATGTCCCATAATGCAATTTAAAAGCATTAAAAACTAATGTTAAGCTTTTTTTAAAATTGTAATTGTTTCATCTTTTTACATTTGCTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16329
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097695 | Nonsense | 794 | 1300 | 16 | 24 |
| ENSDART00000136363 | Nonsense | 765 | 1271 | 15 | 23 |
The following transcripts of ENSDARG00000067824 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 2367376)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 2313255 |
| GRCz11 | 10 | 2340969 |
KASP Assay ID:
2260-2730.1 (used for ordering genotyping assays)
KASP Sequence:
CCTCTAGGTAACTTCTGGAACACTGCCTACTTCAACAAGGAGACRTCATA[C/A]CTGCACTTTCCCACCTKCCATGGGGAGCTGAGCGCAGACATCTCCTTCCT
Long Flanking Sequence:
TATATATCCATACATTCATTTAATTATTCAATGATACATTCAATTATTTATTGATAATTTTTTTATTTGTTTAATTACTCATTCATTCGTTTATTCTTTCACTCACTGGTTTGTTCATTATTTAATTCATTTATTTATTAATTTGCACATTTATTAAATTATTCATTTATTCATTCATTTATTTAAACAATTATTCATTTTCATTTTGACTTAGTTCCTTTTTTAATCTGGGGTTGCCACAGCGAAATAAAGCGGACTTTCTCCAGAAAAAAAACATATTATAGAAAATACTGGGACAAATTGCTTGCTGTGTTAAACATCATTTGGGAAATATTTGAAGAAGATAAATAATAACAGGAAGGCAAATCATTTTGACTTCAGCTGTATGTTTGTAGCGACAGAGTTTTTTGCGATCATGTGAACTGTATAAATGTGCTACAGTAAACATCTCCTCTAGGTAACTTCTGGAACACTGCCTACTTCAACAAGGAGACGTCATA[C/A]CTGCACTTTCCCACCTTCCATGGGGAGCTGAGCGCAGACATCTCCTTCCTGTTCAAAACCAGCTCTTCATCAGGAGTGTTCCTGGAGAATCTGGGCTTCAAAGACTTCATCCGCATCGAGCTGAGCTGTGAGTGTTTTTATCTTCTGCTTTACTCTTTAGTGGGGAATCTCGCCCAAAGAAATGGCATCCTCATATAAAAAGGGTTTTTATTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTATTATTTTTTTTTTTTTATTGAGACAAATTTTTACTTACTTTATTGTCCACAAGTGGAAATTTATATTTGGCACCAGACATCCACATCAGCGTTCACATTACACATACAGTGCATCTGGAAAGTATTGATAGCGCTTCACATTTTCCACTTTTGTTTATGTTACAGCCTTATTCCAAAATGGATTAATTACATAGATTTTCTCAATATTCTACACACAATCCCCCATAATGGCAATG
Associated Phenotype:
Not determined