ZMP
im:6904866
Ensembl ID:
ZFIN IDs:
Description:
transmembrane protein 45A [Source:RefSeq peptide;Acc:NP_001018453]
Human Orthologue:
TMEM45A
Human Description:
transmembrane protein 45A [Source:HGNC Symbol;Acc:25480]
Mouse Orthologues:
2310005G13Rik, Tmem45a
Mouse Descriptions:
RIKEN cDNA 2310005G13 gene Gene [Source:MGI Symbol;Acc:MGI:1916707]
transmembrane protein 45a Gene [Source:MGI Symbol;Acc:MGI:1913122]
transmembrane protein 45a Gene [Source:MGI Symbol;Acc:MGI:1913122]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9025 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40734 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9025
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104157 | Essential Splice Site | 136 | 277 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 6 (position 36777411)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 36851005 |
GRCz11 | 6 | 36828899 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCAATTGCATTAGACCGCATGCTGCTGGCTCTTGCTTTYTTTAATGAGG[G/T]TAGGAACCTGTTTTTTGTTTTTTTAAAACATATTTCCTAATTTTGAAATG
Long Flanking Sequence:
TTTGCAAGCCTACTTATTCTCTTAACTCCAAACTGATAACCACATATTCAGTTATTATTCTACCGACATTATAATGGCTGACCATTGTGGTTGCAGGCATTCATAGTTAACAGAATCTCTGAAGGCGTGCATCAAAATAACATGCTTCTTACTTGTTTTTGCTTCTTATTCATCCTTTTTCACAAAATCTCATTTTGAGGCTACCTGCTGTGAGCTATTTTATTAAGGATTGAAAGCATGTTTGAAACACAATAGCTTAAATGATTGTTCTCCTGATGTTTACACAGGGATGCTAGCGGAGCAACTTTTAGCAGGTGGACCCAAGTTTCAGCTGTATGATTCCTCCACTCAGCACTGGGAGCAGCTGATGAACTGGCAGCACACCACTATGTACCTGTTCTTTGCCATCTCAGGGGCCATTTCTCTCACAGTCCACAGCACAGACATTGCACCAATTGCATTAGACCGCATGCTGCTGGCTCTTGCTTTTTTTAATGAGG[G/T]TAGGAACCTGTTTTTTGTTTTTTTAAAACATATTTCCTAATTTTGAAATGGAGCTAATACTGTGTAAAAGTGTATAGACTATTTTAACATGGTGATGTCATTGGCCCATGAACATTTTCTGCTTATTATCAAAATATTTCATATCTGGAACAATATAAATATACAGTTGAAGAATTATCAGCCCCCCTAAATTATTAGCCCCCCTGTTATTTTTTTTCCCCAATTTCTTTTTAACATAGAGCAGATTTTTTTCAACACATTTCTTAACAAAATAGTTTTTATAACTCATTTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAAATAATATTTTACTAGATATTCTTAAGACACTTCTGTACAGCTTAAAGTGACATTTTAGAGGCTTAATTAGGTTAACTTGGCAGGTTAGGTTAATTAGGCACGTTAATGTATATTGATGGTTTGTTCTGTTGACTATTGAAAAAAATTTTTACTTAGAAGGGCTAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40734
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104157 | Nonsense | 185 | 277 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 6 (position 36779666)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 36853260 |
GRCz11 | 6 | 36831154 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGCCTTCTGGAGGTTTTCCACCGGGGGAATATTCTGCTTGAGCTGCTC[A/T]GAGCAACTCTCACTGTACTGCAGGGCAGCTGGTTCTGGCAGGTCAGTGGT
Long Flanking Sequence:
GCTCATATGACAAGTTTCGCAGTGCTTGGTGAATTCTGACCTGCGAAATCACCAATGGAATGAGATCAAAACATAACCTCTGTACAGAAATTTAAACAAATAGACCAATCACTCACTTTTTTAATGTTTAATCATCTTGTTTAATCTCATGCCTTTTACAACAGAATTTTGCATGCTCAAACTCTTGTGTGTCCACGGTATAAGTGTGTTGAAACAGGGTTGCAACTAAATTATGCAGGGCACCCCTGGATTAGAAGTTCATTAAAACTGCAAGTGTCACTTGTATGTAGAGAAAAATGTATTTTCATAATTTAAAGTACTTCAAAAATCACATTTAAAGTACACTGCCTCTTTCAGGATTCCTGTTCCTTTACCATCTCCATGGTAGAGGCATGCTCGATGTCCACGTGCACACCCTTCTTCTCTATGCCATCTTTGGACAAGCCTTCATTTGCCTTCTGGAGGTTTTCCACCGGGGGAATATTCTGCTTGAGCTGCTC[A/T]GAGCAACTCTCACTGTACTGCAGGGCAGCTGGTTCTGGCAGGTCAGTGGTAGTGACTGCAGGTATTGTACATGCTGTCCTTTCAGTTTCCACTGTTCAACTCTTATCTCTTATTCTTGTGTTTTTCTAGATTGGCTTTGTTCTGTACCCTCCTAGTCAAGTGAAATGGGATCTGGCAGACCACGACAATGCAGTGTTCGTCACATTATGCTACTGTTGGCACCTTGCGTTTGCTTTGCTCACTGTGGCTGTAGTGTACTGGTCTGTCCTCTGGTGAGCATAACAGCTGCTTGAAAATGTCCTGCCAAAAATTACAATTCAGATCTAAAAATTATACTCAGACTCAATTTTATTATCCCATTTAGGGAAACTAAAATTACAACAAAGTGCAATAACAGAGGCGAAGTTCCATGTACACATTACCAAAATATTACCACACAACATACAATACATCATTTTGTAGGTGCATCTCCCTCCCACCCTGGACTCATTTAGTGACTT
Associated Phenotype:
Not determined