Busch Lab

ZMP

zgc:64106

Ensembl ID:
ENSDARG00000011371
ZFIN ID:
ZDB-GENE-040426-1370
Description:
hypothetical protein LOC393348 [Source:RefSeq peptide;Acc:NP_956671]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa11382 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa11382
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
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Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024248 Nonsense 202 309 4 6
ENSDART00000143537 Nonsense 216 323 4 6

The following transcripts of ENSDARG00000011371 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 21 (position 10415502)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 11898865
GRCz11 21 11991493
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGGGGTGAATCGTGTGTACAACCACACCAAGCTGCACAATGTCATCTG[G/A]ACCAACGAGTTGGCACGCAGGCTTCAGGGCACAGGTTCGCAAACTAAAAC
Long Flanking Sequence:
GAATGTTCAGAATTATTTAATAACCCATTAAATTATAAGCCATTATGTGAAATCTGATGATTAATTCTCTGTACCTAGAGTTAAAATGACTCAGTGTTATTTATTTCAAGTGTGAAAAGTCCTTCCTTCTCCCATAAATTCATGATATGTTCTTACCTACAGGCTTACCCATACAGATCACAGCAGATGGGTTGGAAATCACATTTGCAACCAACCATGTTGGACCATTCCTGCTCACCAGTTTGCTTTTAGGTCAACATCCCTAATGTTTATCCTTTCGTTCCAAACTCATCTGGAGGTAACTCACATACAGTAAATGACACCTTTTCTTTTCTTTGTTGCACAGACCTTTTAAAGAAATCCGCCCCGGCTCGCATTGTAAATGTTGCATCCGCAATGCACTGGAAAGGTGACGTGGACTTCGCCCATTTCCATGGGGAGAAACTAAACCATGGGGTGAATCGTGTGTACAACCACACCAAGCTGCACAATGTCATCTG[G/A]ACCAACGAGTTGGCACGCAGGCTTCAGGGCACAGGTTCGCAAACTAAAACTGCATTTGGTCATTGCCAATAGCCTAATGGTTCAGTGCGCTGACATTTAAAACTGAGATGCTCACATAAACCCGAGTCCTGTTCCGCTCTCAATGCTCCCTACACTTTTCTGTCTCTAATCTATTGTCCTATTCAATAAAGCTAAAAAAGAGATATAAAAAAATCCCTTCAAAGCAGCGGTGTCCAAACTGGGTCCTGGAGGGCTGGTGTCCATGAGAGTTTAGCTCCAACCCTTATCAAACACACCTCAAGCAGCTAATCAAGCTCTTACTAAATATACTAGAAAACAAGTTGGAGCTAAACTCCGAAGGACACCGGCCCTCCAGGATCGAGTTTGGAAACCCCTGCTTTAAGGCAAGTCATTTCACTTGGTTGCCATCTTTGACATGCCACTGTGCTCGGGCATTCAATTTCAATGGGGAAACATCAAACTCCCCAAGATTGCTTTCT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa29538
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024248 Nonsense 266 309 6 6
ENSDART00000143537 Nonsense 280 323 6 6

The following transcripts of ENSDARG00000011371 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 21 (position 10409452)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 11892815
GRCz11 21 11985443
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAGACCGCAGAGGAGGGAGCGTTCAGTCCGATATACTGTGCAGTGGCA[G/T]AGGAAAATGAAGGAATAACAGGAAAATACTTTGACAGTGATTGTTCCCTG
Long Flanking Sequence:
AAACGTATTTTTCCATCCTTAAAATAGCAAAAGTGGATTCGAACATGCTCTTAATGATTAAGTGCGATGCCTTTAGACTCTGCGCCTAGATTGTTAAAATAGAGCCCAAGGAGTGATAGTAAAAAACTGACTGGTGCAAATGTGCAAAAACTGGTGTCACTTAGTGTCAGAGATGAACGTCTGCTTTCTACAGGTGGTTTTTCAAACCCACTAATCTGTGTGAGGCACACTCAGAATGTCTTAATGTTTGAGGATTGTTGTGTGGTGTGATGAGGGGAAAGAAGGTTTTGGTTTTGGTTGGGTCCTGGTTTTTTCCACAGGGGTTCAGGTGATTGTGGAAGAGATGAGTTTTTGATTGTAATTGGAATGAAACACACCTTCTAACAAACACATTCATTTAGAAACAGAACTTGTTTCTCATGCACTGACTTTATGTTAATTTTTTTCCACCTCAGACCGCAGAGGAGGGAGCGTTCAGTCCGATATACTGTGCAGTGGCA[G/T]AGGAAAATGAAGGAATAACAGGAAAATACTTTGACAGTGATTGTTCCCTGGTTCTGCCAGCACCTCCCGCCAGAGATCCTGCTCTTGGAGTGAAGGAATATGAGTTCTGTGAGAGACTGATTGCTAAACTGTAAACACCTAGTTCACAGAATGATCTTTTCCATAACGAACAGCTCAAATTTGGTAATTTAATAGCGTTGTAAAGAACACACTGAAATATCAGGTCGCCGCAGCTGTTACTGATTGTTGTAGCTCTGGCCTTTATACAGAGCAGAGCCACCCAGTAAAGTGGTTGTATTTGATGTTACCTTAGCAATGTGATTAGTCTTTTTCAAACTTATTATGAACAGAATGAAGGAGCGCTGTATGAATGTAATGTGAAAAGAGCACAGTCCGGTTCCAGAAGTAAAAAAATAGATTTTTACATTTACTGTTAAAATGTTGAAGGAATATCTGAAGTTGTCAATTGTTTGTATAAGCTTTAGTTGACTCATCTGCTC
Associated Phenotype:
Not determined