Busch Lab

ZMP

zgc:103558

Ensembl ID:
ENSDARG00000002685
ZFIN ID:
ZDB-GENE-041212-23
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]
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]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa2378 Nonsense F2 line generated Not yet available
sa9030 Nonsense Mutation detected in F1 DNA Not yet available
sa11694 Nonsense Available for shipment Available now

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.
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:
sa9030
Status:
Mutation detected in F1 DNA
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

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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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