Busch Lab

ZMP

ENSDARG00000077452

Ensembl ID:
ENSDARG00000077452
Human Orthologues:
AC009958.4, AC110080.2, AC110080.4, AC110080.7, AC110080.8, AC233264.1, AC233264.4, AC233264.6, AC233264.7, IGKC
Human Descriptions:
Ig kappa chain V-II region Cum [Source:UniProtKB/Swiss-Prot;Acc:P01614]
Ig kappa chain V-II region RPMI 6410 [Source:UniProtKB/Swiss-Prot;Acc:P06310]
immunoglobulin kappa constant [Source:HGNC Symbol;Acc:5716]
Mouse Orthologues:
AC140374.1, Gm10878, Gm16634, Gm16688, Gm16797, Gm16798, Gm16800, Gm16904, Gm16955, Gm4964, Gm4965, Gm5153, Gm5572, Gm6827, Gm6832, Igk-V
Mouse Descriptions:
immunoglobulin kappa chain complex variable region Complex/Cluster/Region [Source:MGI Symbol;Acc:MGI
predicted gene 10878 Gene [Source:MGI Symbol;Acc:MGI:3642626]
predicted gene 4964 Gene [Source:MGI Symbol;Acc:MGI:3819952]
predicted gene 4965 Gene [Source:MGI Symbol;Acc:MGI:3648800]
predicted gene 5153 Gene [Source:MGI Symbol;Acc:MGI:3644894]
predicted gene 5572 Gene [Source:MGI Symbol;Acc:MGI:3647785]
predicted gene 6827 Gene [Source:MGI Symbol;Acc:MGI:3648380]
predicted gene 6832 Gene [Source:MGI Symbol;Acc:MGI:3645551]
predicted gene, 16634 Gene [Source:MGI Symbol;Acc:MGI:4439558]
predicted gene, 16688 Gene [Source:MGI Symbol;Acc:MGI:4439612]
predicted gene, 16797 Gene [Source:MGI Symbol;Acc:MGI:4439721]
predicted gene, 16798 Gene [Source:MGI Symbol;Acc:MGI:4439722]
predicted gene, 16800 Gene [Source:MGI Symbol;Acc:MGI:4439724]
predicted gene, 16904 Gene [Source:MGI Symbol;Acc:MGI:4439828]
predicted gene, 16955 Gene [Source:MGI Symbol;Acc:MGI:4439879]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa30316 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa30316
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111300 Nonsense 134 148 2 2
Genomic Location (Zv9):
Chromosome 25 (position 38288333)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 36729356
GRCz11 25 37299915
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACTCTGAGCATCAGTGGAGTCCAGACTGAAGATGCTGGAGATTATTA[C/A]TGTCAGAGTTTACACTGTCCTAGTACTAGCTGTGTGTTCACACAGTGATA
Long Flanking Sequence:
GAGCAGAACAAACACAATCTTCATCATCATCATCATCATCATCACAGCAGACTCAACTACAGCGATGATCAACATCTGCATCTGCATCTGGACCATTGCTGTCTTTATTCATGGTGAGTCTTTCTGTTTAATATGAATGAATTTGATTTTTAGCATTTTAATATGGAAAAGTGATGTATTAAATTGAAATATTAAATAAACCATTTTATTTTCTCTTCTTCAGGATCATCAGGAGTCACTTTGACTCAACCTGAAGTTAAAACTGTCCAACAAGACGAAACAGCGACAATAGAGTGTCACATAGATGTGGGAATATACAGCAACTATTTAGCCTGGTATCAGCAGAAACCTGGAGAAACTCCTAAACTCCTGATTAAATATATAAACAGCCGTTACTCAAACACTCCATCTAGATTCAGTGGCAGTGGAACAGTGAATACTGGAAAAGATTTTACTCTGAGCATCAGTGGAGTCCAGACTGAAGATGCTGGAGATTATTA[C/A]TGTCAGAGTTTACACTGTCCTAGTACTAGCTGTGTGTTCACACAGTGATAAAGCGCCGTACAAAAACCTGCTGTTCACACTGACTGCACTGATTCAGCTGAGAGACACTGAGGAACACACACACACACACACACACACACACACACACACACACACAGCAGCTCTGTCTCCAGAGAGCATGTTCAAACCCAGCAGCTTCACCTCACTGCACTCCAACAAGAGCAACTATTGGGCCTCTCAGTCAAAGCACACTGTTAGATTCAGGCCTTCAGGCAACTCGAGACGCCGATTCTGATGACAAGCGGCTTTATTCAAGCACAACACAAAGACCACAACACAACATGTTCTGCTGAATTCAGTGTGTTGTGGCGTCCTGCTGTGGTGAGGGTTAGGGCTGTCAGATGATTATCAAACCGCTCGTTTCTCTCCGCCGCCATTGTAGTTCAGTCTGAACAGGTCATTAATGATTTGAATAGAGTCAATTTGCCTGTTTGGCCCAT
Associated Phenotype:
Not determined