Busch Lab

ZMP

GIMAP8 (98 of 111)

Ensembl ID:
ENSDARG00000016033
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
sa45579 Nonsense Mutation detected in F1 DNA Not yet available
sa7426 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa45579
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000012832 Nonsense 32 235 1 2
Genomic Location (Zv9):
Chromosome 16 (position 30313820)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 28150958
GRCz11 16 28085581
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTTAGGCTTCCGAAGAGCTGGGAAAAGTTCAGCGGTAAACACCATTT[T/G]AAGCATGGAAGCATTCACTTCGAAGAGAACCACTGTATGTGTAAGAAGAC
Long Flanking Sequence:
CTTTTTTTAGGAGAAAATAACATTATTTATCACATGATTTAATCGTTAACTTTTGTTAACTTTTTATTAACTATTTTTAGAACTTTTACATTCACAAACAGTTGCAGAACCCACTTTATGGAAGGCAGGTAATGGAGCGCTGACGTCTTGTAAAGTTCAGTTCCAAACCCTAGCAGACACACCTGGTTTAGCTAATCGAAATCTTACTAGGCTTTCTAGAAACATCCATGCAGGTGTGTTGAGGCAAGTTAGAGCTAAAATCTGCAGGACACAGAGTTTGAGCAGTCCTGTAATCTAACAATCAAAATACTATATGAGTGGCACCAAAAAAAACAAAGAATTACCAGTACCAGTTTGTAACCTAAAATGTTTGATAGTTGTTGTTCATGTGTGTTATCTTACTTTTTTGTCAGCTCACACTCAAGTGCACATTTCAGAGATGCGAATGATAATGTTAGGCTTCCGAAGAGCTGGGAAAAGTTCAGCGGTAAACACCATTT[T/G]AAGCATGGAAGCATTCACTTCGAAGAGAACCACTGTATGTGTAAGAAGACAAGGTGAAGTGAACGGGACACATGTGACAATAGTGGACACTCCAGGCTGGTGGAAGTGTCTCTCAGTGACTGATACTCCTGAAATGGATAAAGGAGAACTTTTATTCAGTACTGCCCTCTGCCCTCTGTCCACCAAGACCACATGCATTTCTGCTGACTCTGCGATTAGACATGTCATTTACAGCAGAAGAGAAGATGTCAGTGGAGGAACACATGGACCTTTTTGGTGGGCGAGTGTGGACTCATACTGTAGTGCTTTTCACTCACGGAGACTGCCTAGGTGACGTGACTGTTGAAGAGTTTATTGAGGGTGAAGGGGAGGCTCTACAGTGGCTGATTGAGAAATGCGGGAACAGGTATCATGTCATCAACAATGAGAACTGGAATGATGGCAGTCAGGTCACAAACCTGCTGGACAAGATAGAGAGGACGGTTGCACAAAATAAGGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7426
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:
T > C
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000012832 Missense 93 235 2 2
Genomic Location (Zv9):
Chromosome 16 (position 30313621)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 28150759
GRCz11 16 28085382
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTTATTCAGYACTGCCCTCTGNNNNNNNTCCACCAAGACCACATGCAT[T/C]TCTGCTSACTCTGCGATTAGACATGTCATTTACAGCAGAAGAGAAGATGT
Long Flanking Sequence:
AATCTTACTAGGCTTTCTAGAAACATCCATGCAGGTGTGTTGAGGCAAGTTAGAGCTAAAATCTGCAGGACACAGAGTTTGAGCAGTCCTGTAATCTAACAATCAAAATACTATATGAGTGGCACCAAAAAAAACAAAGAATTACCAGTACCAGTTTGTAACCTAAAATGTTTGATAGTTGTTGTTCATGTGTGTTATCTTACTTTTTTGTCAGCTCACACTCAAGTGCACATTTCAGAGATGCGAATGATAATGTTAGGCTTCCGAAGAGCTGGGAAAAGTTCAGCGGTAAACACCATTTTAAGCATGGAAGCATTCACTTCGAAGAGAACCACTGTATGTGTAAGAAGACAAGGTGAAGTGAACGGGACACATGTGACAATAGTGGACACTCCAGGCTGGTGGAAGTGTCTCTCAGTGACTGATACTCCTGAAATGGATAAAGGAGAACTTTTATTCAGTACTGCCCTCTGCCCTCTGTCCACCAAGACCACATGCAT[T/C]TCTGCTGACTCTGCGATTAGACATGTCATTTACAGCAGAAGAGAAGATGTCAGTGGAGGAACACATGGACCTTTTTGGTGGGCGAGTGTGGACTCATACTGTAGTGCTTTTCACTCACGGAGACTGCCTAGGTGACGTGACTGTTGAAGAGTTTATTGAGGGTGAAGGGGAGGCTCTACAGTGGCTGATTGAGAAATGCGGGAACAGGTATCATGTCATCAACAATGAGAACTGGAATGATGGCAGTCAGGTCACAAACCTGCTGGACAAGATAGAGAGGACGGTTGCACAAAATAAGGGGTGTTGTTATGAAATTGACCAGAAGGCTGTAAAGGAAGTGAAGCAGAAACGGAAAGCGGCAGAGAAGAGAGCAAAGGCACGAGCAAGGTATCAGATGAGGAGGATGAAGAGTACTATGAAGGGTAAGATCTAGTACTATGAAGGGTCTGATGAAAACTTGATGACACAAAATAACTCATAAATGCCTTTGAAAGAAATCC
Associated Phenotype:
Not determined