ZMP
hm13
Ensembl ID:
ZFIN ID:
Description:
histocompatibility 13 [Source:RefSeq peptide;Acc:NP_997737]
Human Orthologue:
HM13
Human Description:
histocompatibility (minor) 13 [Source:HGNC Symbol;Acc:16435]
Mouse Orthologue:
H13
Mouse Description:
histocompatibility 13 Gene [Source:MGI Symbol;Acc:MGI:95886]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24231 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24231
Status:
Available for shipment
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:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055142 | Nonsense | 20 | 366 | 1 | 12 |
ENSDART00000128433 | Nonsense | 20 | 366 | 1 | 12 |
The following transcripts of ENSDARG00000037846 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 509380)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 480371 |
GRCz11 | 23 | 493164 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGGAGCAGACCGCGCCGGCGCCCGACGGCTCAAGTAATGGGTCGGATT[T/A]GGTAAACGGGACTGCGGGCCGGTTCGTGTCCAGCGCTGAGGGTACGGCTC
Long Flanking Sequence:
TTTAGCATGTTACTCTGAATATTGGATCTGAATTAGCATGCAAGTATGACTTGTAAACAACATTAACACTGTCTAATTGACTGTGAACAATGCTGTACTTTGATAGTCATTTACTGCTAATATGACTTCCCTATTTTCAATACTTTTCTGACATTATATTATTAAGGAGAATGTCTGAATATCCCAATATACAACCAACCTCACCTCTATGAGTTGACTTCACACTACAGCACAGGAGGTGGCGGTGTAAACCTGTAAAACAGTTTTTTAACAGCCAGTAACCCGCCAGAAGAAGAGGAAGAACACTCACCGGGCTGATTTTAGGAAACGTGGCCTTAACAGCGATCGGTTCCCCCTCAATGAGCAGCGCACTCAGTGACACTCTAATTAAACCGCTTGTATCTAACGTTAAGCCTATCCCGGTAACCGAGCGCGCTGAAACATGGCGGATGTGGAGCAGACCGCGCCGGCGCCCGACGGCTCAAGTAATGGGTCGGATT[T/A]GGTAAACGGGACTGCGGGCCGGTTCGTGTCCAGCGCTGAGGGTACGGCTCTGGCGTACGGCAGCCTGCTGCTCATGGCCCTGCTGCCCATCTTCTTCGGGGCGCTCAGGTCTGTGGGATGCTCCAAATCCAAGGTAAACTCATCTAGATGTCATTCAGATTAGTTGTGATGTTAACGTAAGCGCCACGATTACTTTAAAACCGTAAATACGCAGTCAAACCGATCTGTCGCTGTATGTAAACACCAGTTATCTGAAGCCTGATTTAAAAAACCGTTAACTGAAGCATTTAACGTAAATAACCGTATACTGATGACGCGCGCTCATTTAATCATATTAACAGCACATCATATGATCGATACAATACTGTTGACAGTCAGTTAAATAGTGCTAATGCTTATTTAAATGTGATTTCAGACGCTATATTTAAAGTAACGTTAGCGGTAAACAATATATGGTATAATAATCAATATAATAATACCGTCATTACCTCAGTCAGTTG
Associated Phenotype:
Not determined