Busch Lab

ZMP

GIMAP8 (6 of 111)

Ensembl ID:
ENSDARG00000095531
Description:
GTPase, IMAP family member 8 [Source:HGNC Symbol;Acc:21792]
Human Orthologue:
GIMAP8
Human Description:
GTPase, IMAP family member 8 [Source:HGNC Symbol;Acc:21792]
Mouse Orthologue:
Gimap8
Mouse Description:
GTPase, IMAP family member 8 Gene [Source:MGI Symbol;Acc:MGI:2685303]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa31244 Nonsense Mutation detected in F1 DNA Not yet available
sa39718 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa31244
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
ENSDART00000143063 Nonsense 71 274 3 3
Genomic Location (Zv9):
Chromosome 1 (position 57256147)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150566.1 3993
GRCz11 1 56709440
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGAAAAACTGGAGCTGGAAAGAGCGCGACAGGAAACACCATCCTGAGA[C/T]AAAAGCTTTTTGATGAAAAAGATTCATTAAGTTCCGTGACCAAAAATTGC
Long Flanking Sequence:
AACCCCGGATTAATAAAGGGACTAAGCCGACAAGAATGAATATATATATATATCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGTTCGCATGGGTTTCCTCTGCATGCTCTGGTGTCCCCCACAGTCCAAACACATGAGGTACAGGTGAATAGGGTAAGCTAAATTGTCCAAAGTGTATGAGTGTGAATGAGTGTATGTGGATGTTACCCAGAGATAGACTGCAGCTGGAAGAGCATCCGCTGCATAAAACATGTGCTGGATATGTTGGCGGTTCATTCTGCTGTGGCGACCCCAGATTAATAAAGGGACGAAGCCCAAAAGAAAATTTATTATTATTATTTCTTTAATTGAAATATTATTAAACTTTTTTTTTCCTCAGACTCTGCCAAACACAGACAATTAAACTCTGGCGAATGCGCAGATCTCAGAATCGTGATGGTGGGAAAAACTGGAGCTGGAAAGAGCGCGACAGGAAACACCATCCTGAGA[C/T]AAAAGCTTTTTGATGAAAAAGATTCATTAAGTTCCGTGACCAAAAATTGCCAACAAAACCAGCACACGGTCAATGGCAAATCCATCACTATCATCGACACTCCAGGACTGTGTGATACGTCAATCAGCGAAGAAGAGCTGAAGAAAGAAATCGAGAAATGCGTTGAGATGTCTGTTCCTGGCCCTCACGTGTTTCTGCTGGTGCTCAGACTGGACGTCAGACTCACAGATGAAGAGATAAACACAGTCAAATGGATCCAGGAGAACTTTGGAGAAGAAGCTGATCGATACACCATCATCCTCTTCACTAGAGGAGATCAGATTAAAACACCCATAGAGGAGTTTCTGGCAAATAACAAGCAGATGATAGCACTAGCTGAACAGTGTAAAGGTGGATATCATGTCTTCAACAACACAGATGAACAAAACAGATCTCAGGTCAGTGAGCTGCTGGAGAAGATCGAAAAAATGGTGGAGAAGAACGGAGGACGGTTTTACACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39718
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000143063 Nonsense 197 274 3 3
Genomic Location (Zv9):
Chromosome 1 (position 57256525)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150566.1 4371
GRCz11 1 56709818
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCCATAGAGGAGTTTCTGGCAAATAACAAGCAGATGATAGCACTAGCT[G/T]AACAGTGTAAAGGTGGATATCATGTCTTCAACAACACAGATGAACAAAAC
Long Flanking Sequence:
TTTTTTCCTCAGACTCTGCCAAACACAGACAATTAAACTCTGGCGAATGCGCAGATCTCAGAATCGTGATGGTGGGAAAAACTGGAGCTGGAAAGAGCGCGACAGGAAACACCATCCTGAGACAAAAGCTTTTTGATGAAAAAGATTCATTAAGTTCCGTGACCAAAAATTGCCAACAAAACCAGCACACGGTCAATGGCAAATCCATCACTATCATCGACACTCCAGGACTGTGTGATACGTCAATCAGCGAAGAAGAGCTGAAGAAAGAAATCGAGAAATGCGTTGAGATGTCTGTTCCTGGCCCTCACGTGTTTCTGCTGGTGCTCAGACTGGACGTCAGACTCACAGATGAAGAGATAAACACAGTCAAATGGATCCAGGAGAACTTTGGAGAAGAAGCTGATCGATACACCATCATCCTCTTCACTAGAGGAGATCAGATTAAAACACCCATAGAGGAGTTTCTGGCAAATAACAAGCAGATGATAGCACTAGCT[G/T]AACAGTGTAAAGGTGGATATCATGTCTTCAACAACACAGATGAACAAAACAGATCTCAGGTCAGTGAGCTGCTGGAGAAGATCGAAAAAATGGTGGAGAAGAACGGAGGACGGTTTTACACCAATGAGATGTACGAGAAAGTTCAGAAGAAAATCAAAGACGAAGAAGAGAGACGACGAGCGGAGGAAAAACGACTGAAGGCAGAAAAGAAGGAAAAGATGAGGGCTGAAGAGAGAAGTAAACTGATGAAGGAGGTCGCGGTGGGAGCAGCAGTGGTCGGCGGTGCAGCATTACTTACTACAGGAGGACCGATCTCTGAAACTTTATTTTTAGCAGTTGGAGACGCAGCCCTGTCCTCCTGTGGCACAGCTATATTGACGGGAGCAGCAGCTCTTGGAGGCGCAGCACTATCAGCGGTCACCGGAGGCACACCTACTAATTTAATAACAAGAGGAACTTTTACAAACATTCAGATCTCACCTAACGCTCCCCAAGATCCA
Associated Phenotype:
Not determined