ZMP
zgc:103558
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC494057 [Source:RefSeq peptide;Acc:NP_001008600]
Human Orthologues:
FAM113A, FAM113B
Human Descriptions:
family with sequence similarity 113, member A [Source:HGNC Symbol;Acc:16212]
family with sequence similarity 113, member B [Source:HGNC Symbol;Acc:28255]
family with sequence similarity 113, member B [Source:HGNC Symbol;Acc:28255]
Mouse Orthologues:
Fam113a, Fam113b
Mouse Descriptions:
family with sequence similarity 113, member A Gene [Source:MGI Symbol;Acc:MGI:2442177]
family with sequence similarity 113, member B Gene [Source:MGI Symbol;Acc:MGI:2446270]
family with sequence similarity 113, member B Gene [Source:MGI Symbol;Acc:MGI:2446270]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2378 | Nonsense | F2 line generated | Not yet available |
sa11694 | Nonsense | Available for shipment | Available now |
sa9030 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2378
Status:
F2 line generated
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012483 | Nonsense | 72 | 415 | 4 | 10 |
ENSDART00000131530 | Nonsense | 72 | 295 | 4 | 8 |
ENSDART00000139455 | Nonsense | 72 | 196 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 7 (position 26002935)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 24564687 |
GRCz11 | 7 | 24835844 |
KASP Assay ID:
554-3205.1 (used for ordering genotyping assays)
KASP Sequence:
CCTTGGTGGAAGGAGGCAGACTGGGGGAGATGAATAATGGGACACAATAC[A/T]GAGAAGTTAGACAATACAGAACGGACCACCACTTGGTCCGCTTTTACTTC
Long Flanking Sequence:
TTGTTGCCAAAGGGTTTGCATAAGAGTTTATCTAAGCTGTGTGAACATTCAACACTGCCTTGCTTTACACTGAATGTGTTCAGCTGAACTAGAATGACTAAATTTAAACTAAATATGTAAAAACTAAATAGAAATATGTTCACAACATAAAAACTAAACTAAAAAGTATTCATTAATATAGTTAACTAAACTGAAATTTACAGCAAAATGAAAACTGAAAAGCTGTAATAACCTTTATACAAAAGCAGTTTATTCAAAAGAATTAACATCATCAGTTTTTGTTTTATTTTTATTTCATGTAATTTATTAAACCAAACATATAAATGTGGAAACAAGCTGCTGTGTATGTTTAGGATTAAGGACAGAATTTTTTTCTTTTCCCGGTATAAGCACGGTCTGATATCTGTTCTTTCCCTATTTCCCAGGGTGAATTCTCATTTGAAAATGACACCTTGGTGGAAGGAGGCAGACTGGGGGAGATGAATAATGGGACACAATAC[A/T]GAGAAGTTAGACAATACAGAACGGACCACCACTTGGTCCGCTTTTACTTCATTACCCGGACGTTCTCGCAGTATGTGGAGAGCATCATCTCTGACTTTGAGAAGGGAATAAAGCCAGACCTGGTGGTGGTGAACTCTTGTGTGTGGGATATTTCCAGGTGGGACTGCTCCTCATTACAGCCTCTTACAGATATACGGTGTTTAGCATGTGGATTTAACGAGATTTTACTACATTTCACAGGTACAGTCGACAGTGGGCTGTGGAATACAGGGAGAACCTGAAAAAGCTCTTCATGAAGCTGAAGAGTGTTTTGCCTGAGGAGAGCCTGGTGATATGGAATATGACCATGCCTTTGGGCAGGAAGATCTTAGGAGGTTTCTTGGTTCCTGAGGTGGGTTTAAAAATGGTAGAGGATTAAACTTCATTAAAAAACAAAGATTATAATCCATGATATTTTTTCATATCTTGTTCCCAATCTCAGATAGAGCACATGGGCCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11694
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 |
---|---|---|---|---|---|
ENSDART00000012483 | Nonsense | 266 | 415 | 7 | 10 |
ENSDART00000131530 | Nonsense | 266 | 295 | 7 | 8 |
ENSDART00000139455 | None | None | 196 | None | 5 |
Genomic Location (Zv9):
Chromosome 7 (position 26001964)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 24563716 |
GRCz11 | 7 | 24834873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCTTCATGCAGATCAGCAGGATTCTAAACCAGCAACCCAGCAGAACCGA[C/T]AAAGCGGGCTTTCAACTCCTCCTGTGCGCTATAGAGGTAYACTGTCAATG
Long Flanking Sequence:
CCCAATCTCAGATAGAGCACATGGGCCCATCGTTAAGATTTGATGTCATTGAAGCGAATTACTTTGGAGCCACACTTGCCAATGAGTCTGGCTTTGATGTGCTGGACCTCCATTACCAGTTTCGTTTCAGCCTGCAGCATCGAACTCGTGATGGTGTCCACTGGAATGCTGTGGCTCACCGGAAACTATCATCCCTTCTGCTGCAACACGTCGCAGAAGCATGGGGTGTTGAACTGCCGAAGCTAGGTGAGAAATGCAGGTTGAGTTGGTGCTTCTGGTTGGCAAAATAAAGTAATTTTGTTATAGATTGTTTGCTGGGGTCCCAGAATGATGATGAGAATGTTATTGTTTTCTCTCTCTTTATACTAACTGAATATTACAGATAATCACATTTGCAAAAAAATGACTTGGTTAAGGATGCATGGAACATAGTCACAGATCTGTTTTGTTGTCTTCATGCAGATCAGCAGGATTCTAAACCAGCAACCCAGCAGAACCGA[C/T]AAAGCGGGCTTTCAACTCCTCCTGTGCGCTATAGAGGTACACTGTCAATGGGCTGAGAAGTTTCTTTTTGTTCAATTATGTGAACACAGTGTATAATTGATATGCACATATGAATACACATGTATTTAATGAAATAGATGATGTTTACATGTGTGTGCTTAGATAATGTAATGTTTTATTAATATATTTGTATATAAAGAGTTCAGATGCAAAAGCTGCTAAACGTCAGTCACTTCAGCCAAAAATGAACTAATGACATTGAGTGAATGCTTTAGGCACGTACTACACCATCAACAAACAGTTTTGCTTCAAATCATTTAAATCTCAGCGTTAGCACATTCAGAAATGTTTGTTTGCAAAAGCCTCTAAACACCACGCCGGCTTTTATGAGGAGACTGTTTTATTCTGATTTAGATTTTAAAAGCTGGAGTTTGATGAATTGAATGAGCCTGTCTGACTGTCAGTGAATGGCAAATGAAAACGTCTCTTACCTCAAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9030
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012483 | Nonsense | 266 | 415 | 7 | 10 |
ENSDART00000131530 | Nonsense | 266 | 295 | 7 | 8 |
ENSDART00000139455 | None | None | 196 | None | 5 |
Genomic Location (Zv9):
Chromosome 7 (position 26001964)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 24563716 |
GRCz11 | 7 | 24834873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCTTCATGCAGATCAGCAGGATTCTAAACCAGCAACCCAGCAGAACCGA[C/T]AAAGCGGGCTTTCAACTCCTCCTGTGCGCTATAGAGGTAYACTGTCAATG
Long Flanking Sequence:
CCCAATCTCAGATAGAGCACATGGGCCCATCGTTAAGATTTGATGTCATTGAAGCGAATTACTTTGGAGCCACACTTGCCAATGAGTCTGGCTTTGATGTGCTGGACCTCCATTACCAGTTTCGTTTCAGCCTGCAGCATCGAACTCGTGATGGTGTCCACTGGAATGCTGTGGCTCACCGGAAACTATCATCCCTTCTGCTGCAACACGTCGCAGAAGCATGGGGTGTTGAACTGCCGAAGCTAGGTGAGAAATGCAGGTTGAGTTGGTGCTTCTGGTTGGCAAAATAAAGTAATTTTGTTATAGATTGTTTGCTGGGGTCCCAGAATGATGATGAGAATGTTATTGTTTTCTCTCTCTTTATACTAACTGAATATTACAGATAATCACATTTGCAAAAAAATGACTTGGTTAAGGATGCATGGAACATAGTCACAGATCTGTTTTGTTGTCTTCATGCAGATCAGCAGGATTCTAAACCAGCAACCCAGCAGAACCGA[C/T]AAAGCGGGCTTTCAACTCCTCCTGTGCGCTATAGAGGTACACTGTCAATGGGCTGAGAAGTTTCTTTTTGTTCAATTATGTGAACACAGTGTATAATTGATATGCACATATGAATACACATGTATTTAATGAAATAGATGATGTTTACATGTGTGTGCTTAGATAATGTAATGTTTTATTAATATATTTGTATATAAAGAGTTCAGATGCAAAAGCTGCTAAACGTCAGTCACTTCAGCCAAAAATGAACTAATGACATTGAGTGAATGCTTTAGGCACGTACTACACCATCAACAAACAGTTTTGCTTCAAATCATTTAAATCTCAGCGTTAGCACATTCAGAAATGTTTGTTTGCAAAAGCCTCTAAACACCACGCCGGCTTTTATGAGGAGACTGTTTTATTCTGATTTAGATTTTAAAAGCTGGAGTTTGATGAATTGAATGAGCCTGTCTGACTGTCAGTGAATGGCAAATGAAAACGTCTCTTACCTCAAAACT
Associated Phenotype:
Not determined