ZMP
si:dkey-19p15.9
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8JIW6]
Human Orthologues:
FAM178A, FAM178B
Human Descriptions:
family with sequence similarity 178, member A [Source:HGNC Symbol;Acc:17814]
family with sequence similarity 178, member B [Source:HGNC Symbol;Acc:28036]
family with sequence similarity 178, member B [Source:HGNC Symbol;Acc:28036]
Mouse Orthologues:
Fam178a, Fam178b
Mouse Descriptions:
family with sequence similarity 178, member A Gene [Source:MGI Symbol;Acc:MGI:1924968]
family with sequence similarity 178, member B Gene [Source:MGI Symbol;Acc:MGI:3026913]
family with sequence similarity 178, member B Gene [Source:MGI Symbol;Acc:MGI:3026913]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15823 | Nonsense | Available for shipment | Available now |
sa13972 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15823
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058065 | Nonsense | 188 | 1212 | 3 | 20 |
ENSDART00000136689 | None | None | 363 | None | 11 |
Genomic Location (Zv9):
Chromosome 13 (position 8988100)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 9290720 |
GRCz11 | 13 | 9622743 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGGCGCAAWTCACTCTTAWTCCAGCAGAGACCGAGRAACTCATCCGGG[C/T]AATTCACCCACAACCCCAATCAGAAAAAAGACAGAATGGATAATAGAGAT
Long Flanking Sequence:
ATTAATAATAATAATACCTTTTCAACTTTTATTTACTCCTTGTATACTGTTCAAATTGACTACCGTTTTGTTATATTTATGGCAGTTTTAGCCCCATTGACTTCCATTATAATGCCTTTTTTTTTTTTTTTTAAGCCATGACAGGATAAAATCATGCATTCCTGATTGTTTGTGGTTTTTCCTATTGGGGGTAGGTAAATGTGTGGGCCTACTAAAAAGACTAGAAATGCCTAGAAAACAGGAAATTAGAAACTGTCAATCTGATTTTTCTTGCGGTAGTTATAATTGTTATACAGTACTTTAAATTTGAACTGGTGTCTGCTTACTGGAACCAGCACTCGCTAATCCATGTTCCCTGTGTACAGGTTAGAGGAGGTCTGTTTCAGTCAGAAAGTGCTGTGAAAGCTCGGAGACACACTCTTCCTCACTCATCTCACAGACGAAGTCCTGAGAGGCGCAATTCACTCTTATTCCAGCAGAGACCGAGGAACTCATCCGGG[C/T]AATTCACCCACAACCCCAATCAGAAAAAAGACAGAATGGATAATAGAGATCATAAAACATCCATAAAGAAGGTAAAGTTCAGTTGAAACTCGTTTTAATGAAATGTTATCATGAAACCTTAAAAAAAACAAGATTTCTACTCTTTTTATTGGATGTTTTATAGGAGTTGAACAACTTGAACACGATGACTAGTCCAGGTAAAAATAGTTATCATATTAATCATCCCTGATTCTGCTTTTTTTGCCATTCTAAAACTAATCTAGCTCTCTATCTATGTCAAATACCCATTTTTGCCAACAGAGGGCAGACTGTCCTTATCTGCAAAGAGAAAAAGCGAAGCCAGCACAGGGAGTGAGAGGGAAACAAAACGGCCACGTGTTGATATTCAAGCCACCTCCAGCTCTTCTATATTGAACTCGCCTCCAAAGTTTATCAGACGTGCTTTCCTGAAGTCCTGCAATGAGTCCGTTATAACCATAAAGGAGACAAATTCCCCTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13972
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058065 | Essential Splice Site | 922 | 1212 | 15 | 20 |
ENSDART00000136689 | Essential Splice Site | 216 | 363 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 13 (position 9009314)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 9311934 |
GRCz11 | 13 | 9643957 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTTTGAAWCACACCTGCACTTATAATCCCTCGGGCACAGATTTTAAGG[T/A]GAGAATAATTCATTCAATATCAGCTGCTTTTTGATGTTKACAATTCAGCT
Long Flanking Sequence:
TTTGGAACTTTGCTCATTAATTGTCATTCATTTATTTATTTTTTTAATCTGTGTTTTCTTTTATGGTGAATGGAAGAAAATCAAAAAAGGAAAACAAAAAACATTGACTGAGTTTTTATTTTTGTGTGTACTATCCATTTAGTTTAACACAACTTTCTCTCTCTCTCTTTTAAAAATATGTCTAGATATCGAAAGCTTGCCAGATCTTGACCGATTTGTCAGAAGACCATCACAACCTCAGGAGAATCGTTTCTATTCTGCCTGAGAGCAGTCGTGGAAAGTGAGTGAAATCCTGTAATGCAATATTCAGCTTGTTGACCTTTTATTATAGACCATAAAGATGATGAGGCGAATCAACATTTGCTCTCAGGGCTTCATGTAACTATTATTCATCTGCTGTTTCATCAACAGGCTGTTAAAACGACACTTAAGCGTGTCTATCATCTCAAAGCTTTTGAATCACACCTGCACTTATAATCCCTCGGGCACAGATTTTAAGG[T/A]GAGAATAATTCATTCAATATCAGCTGCTTTTTGATGTTGACAATTCAGCTTCAATTAAGATGCTTTATGATCTGTGATGAGTGAAATTATGCAGGTGCATGGTTCACTCAGAAGACCATGCTTTGTTATTTTTGAAATAATAATACATGCAGTGGCCAGCATAAATGTGTACACCTCTTACAAATCTCTTTTAGACAAATACTTTACACAATAAGATAATTGTGTACAGTGTATACAATACATTACCTTGGTCAATACCAAAGCCCAAATTGGAACTGATATACAAAATAACTTAAGTGTGTATGTTTCCATGAATAAACTGTGAAAACTGCTGGGATTCACATAGTTCCTACATGTTGTCCCAACACAAATCAATTAAGTTAACTTAAAAATGTTTAAAAACTTGGTCCCACTTTATATTAAGTGTCCTTAACTACTATGTAATTACATCAAAAAAAAAAAAATACAATGTACTTACTGTGTTCATAAAGTATTTAAGA
Associated Phenotype:
Not determined