Busch Lab

ZMP

zgc:153723

Ensembl ID:
ENSDARG00000007769
ZFIN ID:
ZDB-GENE-060929-978
Description:
hypothetical protein LOC767718 [Source:RefSeq peptide;Acc:NP_001070124]
Mouse Orthologue:
Sult5a1
Mouse Description:
sulfotransferase family 5A, member 1 Gene [Source:MGI Symbol;Acc:MGI:1931463]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa41043 Nonsense Mutation detected in F1 DNA Not yet available
sa7605 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa41043
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
ENSDART00000020851 Nonsense 81 311 2 7
ENSDART00000138714 Nonsense 81 311 2 6
Genomic Location (Zv9):
Chromosome 7 (position 57869581)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 56304907
GRCz11 7 56606318
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGACTATTGCCCAAAGTCAACCTAACTGGGCTCGTGCTCCATGGCTTGAG[C/T]AGTACTACTGCCCTGAAGTTCTGAAAGCATCTTCTGGACCTCGCATTATT
Long Flanking Sequence:
TCTTAGTGACGTGTCACTTCCTTTTTTTTTTGTCTATAAATTAGTTGACAGCAATGTCAGTACCTCAGACCTTTTAGTTCAATAATTCTTTTTCAAACATTGAATCACGTGCAAACATGTCTCGACTAGATGTCACAGAATCTTTTCAGGGCATCAAGTTTCCTGGGCACATGCATACTGAAGAATCCCTGAATTTTGCAACTGACTTCAAGTTTGAAGAGACAGATACTCTGATAGTCACCTACCCCAAATCAGGTAATAACAAAATTATTTTCTGTATTTATTTTTAAATAGCAGGTTTTCATGGTTTGTGTATTTCATCTTTCATTCATCTTTTTTCCAAGCAAGAAATTGCTCATGAATTCATTTTCTCCTTGATTGAATTATTTTGCCTTATAGGAACCACATGGATGCAGGAAATCCTCACTCTGGTTTTGAGTAAAGGGGACCCGACTATTGCCCAAAGTCAACCTAACTGGGCTCGTGCTCCATGGCTTGAG[C/T]AGTACTACTGCCCTGAAGTTCTGAAAGCATCTTCTGGACCTCGCATTATTACTACACATCTGCCTTACCATCTGCTGGCACCAGCCCTGCAACACTGCAAAGCAAAGGTAAGAGGATGGGCAAGACACACACGATGCACTGTTTAGTTTTATTAATTAAACTCATACCCAATGATGGTTTTACTACTATGTACATGAAAATGTAAATATGTAACAATTGTTAACACATTTTGGCCATTCACTAACACGATAACCACTGTTTACAGTCAAGCCTGAAATTATTCATACCCCACAAAGTTAACTCAAAACTGTAAGGCAACTTGCTGGACAGCAGATTTTATTTTGACTTAACTTTTAGCCCAAGTACTACACTTAACTCTATTTAAATAAGTCAGCTTAAAAACTATTCATCAAGTTGCCTTACAATTTAAATCTACTTTTTTATAGTACTTTGTGCTTAATAGTACCATATACCATATAAAATTGTTTATAATTACAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7605
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000020851 Missense 146 311 3 7
ENSDART00000138714 Missense 146 311 3 6
Genomic Location (Zv9):
Chromosome 7 (position 57868368)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 56303694
GRCz11 7 56605105
KASP Assay ID:
554-4161.1 (used for ordering genotyping assays)
KASP Sequence:
TTCATATTACCACTTCCACAAGATGGCAAATTTTCTCCCTGACCCAGGAA[C/T]GTTCCCTGAGTTTCTRAAGAATTTCCTAAAGGGTGAYGGTTAGTTGATGT
Long Flanking Sequence:
GAATGTGAAATAAAATCCTGCATGTATGCATGCATATATAAGTACTAATAAACAGCCAATATCTAAACAACAAATAACAACTTCACTCGCTATTTGTGTTTATTAGTATTTTTTTAACAGTTCAAGCTATTTAAATGTCATAAGATGGTGTGCTGAGATGCGGTTATTTCTCTGCAGGCTTTGGGTGTGAGTTCACAGAAACCCGCTATACTGGCCTGGGGTGCATTTCCTACAGACAAATTCCATCATGAGCAATGGAACTTTTGACAATAGTTAAATAATGATGCTTTTGAGGAATACACCCTGTCATGCATATTAAAGAATTTTCAGTTATGATGATAACCAAAATGTATTTCTGTTGAATTTACTGTGGTGACATGTTTGCAAGTAATAATTGTTTGTCTTTCCACAGGTGATATATGTGGCAAGAAATGTCAAAGATGTGTGTGTTTCATATTACCACTTCCACAAGATGGCAAATTTTCTCCCTGACCCAGGAA[C/T]GTTCCCTGAGTTTCTGAAGAATTTCCTAAAGGGTGACGGTTAGTTGATGTTTATATTATCAGTCAAATATTCCCATAGTGTTTTTTTTTTTTTTTTTGTCTGTTGTAAAAATAATTTATGGCTCTTTTTTTTTTTTTTTTTTTGCAGTGCATTATGGATCTTGGTTCGATCATGTCAACGGCTGGACCGGTCATGCTAAAAACTTTCAAAACTTTTTTTACATCACTTACGAGGAAATGTTTCAGGTAGGATTACTTCATTTATCAGTATTTGGAAACCACATACATACTGTATATGACCCTGGACCACAAAAACATAAGTCATAAGTATTATATATTAATTTATTTATTGAGATTTATATGTCATCTAAAAAGTTAATTTAAATCTGATTAAGTAAGCTTGGCATTGATGTGTGGTTTGCTAGGATACATGTCAATATTTGTCCAAGATACAACTATTAAATCTGGAATCTAAGGGTTCAAAAAAATCTAAATACTGAG
Associated Phenotype:
Not determined