ZMP
NP_001012260.1
Ensembl ID:
Description:
XK-related protein 5 [Source:RefSeq peptide;Acc:NP_001012260]
Human Orthologue:
XKR5
Human Description:
XK, Kell blood group complex subunit-related family, member 5 [Source:HGNC Symbol;Acc:20782]
Mouse Orthologue:
Xkr5
Mouse Description:
X Kell blood group precursor-related family, member 5 Gene [Source:MGI Symbol;Acc:MGI:2442327]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29464 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37161 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa29464
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000097881 | Nonsense | 198 | 621 | 5 | 11 |
ENSDART00000123762 | Nonsense | 223 | 633 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 48771774)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 47623154 |
GRCz11 | 20 | 48100469 |
KASP Assay ID:
2261-4937.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGGCCCGCTTCACCAGCCTCGCCCTGTTCACCCGCACCTTCGGCTGCT[G/A]GCTCATCGGGGTCATCGGTGAGTCTGAGACACAGGAGATTATATACATGC
Long Flanking Sequence:
GCATTAGCTCGGGCATCCTGAAAAAAATGCAGATTTTGTTTGATTCAAACTTTTAGAAACAAAACTTGACAGTTGTTGCTTCATTTTATTGGTGATTCTAAATATGTAATGTAATAATAAGTTTGGCAAACAGTTTTGAAGAATTTGGTGTTTCCCCATTCAGACAGAATGCCCGAGCATACTGCACGAGAGGCATTTCAAAGATGGCCGCCGAGTAAAATGACTTTCCCTAAAGGGACTTTGATGTAACTGGGAGATAATAATTGTATTGTGTGCTCTCCTCCCCTTTGTGTTTCTGTCTGCAGTGGCTCTGTGCAGTGGTGTGTGTCTGCTGTCTCTGTCGTGGGCGCTGGTGCTCTACAGTCGGGCCTGTTGTCTGATTCGTCCTGGGCATTTGCAGATGCCGCCGGCGGCTCTCCTCAGCCAGCTGCTGTGGAGAACGGGCATGTTAGCGGCCCGCTTCACCAGCCTCGCCCTGTTCACCCGCACCTTCGGCTGCT[G/A]GCTCATCGGGGTCATCGGTGAGTCTGAGACACAGGAGATTATATACATGCACATGGTCAAGTTTTGTTGAAGTTAAAGTCTGAATTATTAGCTCTCCTGAATTAATATCTCCTTTGTATATTTTCCCCCGAATTTCTGTTTAACGGAAAGAAGATTTCTTCAACACATTTCTAAACATAATAGTTTGATAACTCATTTCTAATAACTGATTTATTTTATCTTTGCTATGATGACAGTATATAATATTCGACTAGATATTTTTCAAGACACTTCTCTTGCACGCCATTACTCTGCCTCTCTCGCTCCAATACTCGACGTCTCTCCTGTGCCAATACTCGGCCTCTCTCCTGCGCCAATACTCGGCCTCTCTCCCGCGCCAATACTCGGCCTCTCTCCTGCGCCAATACTCGACCTCTCTCCCGCACCAATACTCGGCCTCTCTCCTGCGCCAATACTCGGCCTCTCTCCCGCACCAATACTCGGCCTCTCTCCCGTGCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37161
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000097881 | Nonsense | 207 | 621 | 6 | 11 |
ENSDART00000123762 | Nonsense | 232 | 633 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 48774436)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 47625816 |
GRCz11 | 20 | 48103131 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCTCCCAATTCATGTGATGTATGCTTCTATTTCTCAGCGTCTCATTG[G/A]CTGATGGCAGCGCTGTGGTTGGTCTCCCAACAGACGGACATATATGTAGG
Long Flanking Sequence:
AAAAGGTGCAATATGCAAACGGCCACTAAAAGGCCGCCGTCCTTGGCGAATCTCCAGCAGTTGATCATCTTTTTGCACAGACATGGTGGATTCACCTGATTTGTTGACAAACGGGTTGCAGATCCATTCCTCTGCATTTTGTGGGTCCTCCTCTGGGCCTTTTCCCCCTAGCAAAGAATCTTTCCAAAGACGTCTTGTTTCTTACTCATTTTGCTGCTTGTGGGCTAAATTTAGGCAATTAAGTGACCGAGATGTAAGCGTGAGAATACAGTCATTTTTCTAAATAAAAGATCGTTCACTCGGATAATAAATAAAACAGAAATAATCAATGATTTATTGTGCGGCCCGTTACCGATTGATCCAAGAACCGATACCGGTCTGCAGCCCGGTGGTTGAGGATCACTGCTCTACAGCATTTTGTCAGATACCAAACACAATAATATCATTAACTCATCTCCCAATTCATGTGATGTATGCTTCTATTTCTCAGCGTCTCATTG[G/A]CTGATGGCAGCGCTGTGGTTGGTCTCCCAACAGACGGACATATATGTAGGCCAATGGTCATGGCGGGTGTTTAACTTCATTCTGGGAGGCGTTCATGTGTTTCTGTTCCTCAATGTGAAGGACGGTCCGTCCCGCTTCCGGATGGCAGGATTCTACACGGTACAATCACACTAATAATGTTGTGCTTTTTTAGATTTGGCTGTATTTGGGTTAAAGTCCACATGAACCAGAAGCTGCGACCGTTTTTTTTTTTTTTTCATATTGTGATATGCAGCTCCTAGGGAAATGGAATATTAAATGAGAAAACAGTGGGCGTGACTTGTTTTTCTACTGCGAGCTGATTAGATAAAGTAAAGTAGGCATTTTATAAAGAAAGATTGGGAAATGGGTTTCAGGAGAGTTCTTACAACCTAAAAGACACCTCCTGCTCAGCATTTCTGTTTGTTGTCAAAACTCAGAAAATACGTTGTTAAAGAGGGAGGAGATGATTTGATTAAAGG
Associated Phenotype:
Not determined