ZMP
GIMAP8 (98 of 111)
Ensembl ID:
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.
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.
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