ZMP

XKR8 (3 of 4)

Ensembl ID:

ENSDARG00000004498

Description:

XK, Kell blood group complex subunit-related family, member 8 [Source:HGNC Symbol;Acc:25508]

Human Orthologue:

XKR8

Human Description:

XK, Kell blood group complex subunit-related family, member 8 [Source:HGNC Symbol;Acc:25508]

Mouse Orthologue:

Xkr8

Mouse Description:

X Kell blood group precursor related family member 8 homolog Gene [Source:MGI Symbol;Acc:MGI:2685877

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39246	Nonsense	Mutation detected in F1 DNA	Not yet available
sa36841	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39246

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000104033	Nonsense	167	397	3	3

Genomic Location (Zv9):

Chromosome 19 (position 25469170)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	25399282
GRCz11	19	24983505

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTGCTTATGTAATCTTGTTTACTAACTATGCTGTTTCATCATTTCAGGTT[T/A]AAAATTTCTCACATCAGCTGCTTCAATTGCCAGTTCTCTTGCCATGTACC

Long Flanking Sequence:

GGAAGGAACAGAAATGCTACTGTAGATGAAATCAGATGACAAGTAGCCTCCTGCCACCTAAAACACACTTACAACTGCTTACGGCCTTACTCCAGCCAAACCATTATGCCCACTTTATGGGATATGTCACATATTTTGCTCACAGTCTATGTATAGTTAGCCAAAATGGTTTCCAAACAAAGTTTTCGCATTTGCTGGTTCTATCAGCTTTTAATTAAATAATGTGTATTTACGACAGTATTCATGATACTTATAGCAGCCAATTGCATTTATCTTCCACATGCCATGAACAAAAAAATCACACAGTGTTGGTTTAAGTATAGTTTTGAAATACTGTCCATCCCCGGCACCATGTGTAGGCAGTGCCTAATGAGTCATTGAATAATTCACCCAAACCATTTACATGTTATGATTAAATGCATCACTCACTTTTTCAAAAGAACTGCATTCTTGCTTATGTAATCTTGTTTACTAACTATGCTGTTTCATCATTTCAGGTT[T/A]AAAATTTCTCACATCAGCTGCTTCAATTGCCAGTTCTCTTGCCATGTACCACAACGGCATTCGGATTTGTTTTGATGTAAAATGCTGGACCGCCACTGCTGTCTATTTGCTGTGGAACTTTCTGCTGATCTTTCCCCGTGTGGCCGCTCTGGCACTCTTCTGCAGTGTATTCCCGTGCCACATCGTTGCTCATTTTCTATCTTTGTGGATGGTGCTGGTGTTTGTGGCCTGGAGACAGAAAACAGATTTCATGGAAAGCAGCGGCTGGCAATGGCTTTTCAAAGCTACAGTTGGACTCATCTGGTATTTCAGCTGGTTTAATATCTCAAAAAGTAATACAAAGTTAAAGCATGCCATTTATTGTAGCTTCTTGCTGTTAGACATGATGATGCTTCTGGGCTTCTGGAGTTGGAAGGTGACCGAGTATGCAGGCTGCTGGACCTCTTTAAACCCTGCTGTAGTTATCCCAACACTACTAGGATTGTATATCATTGGAAATC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36841

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000104033	Nonsense	389	397	3	3

Genomic Location (Zv9):

Chromosome 19 (position 25468505)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	25398617
GRCz11	19	24982840

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCATTGAGACAGAAACTGTAGATGAAGTTCCTGGAGTTCTCCTTCGAAGT[A/T]AAATCATGGCAGCAGATTTCTGCTTTTAGTTCTTAATTCAATTGTACAAA

Long Flanking Sequence:

GTGTATTCCCGTGCCACATCGTTGCTCATTTTCTATCTTTGTGGATGGTGCTGGTGTTTGTGGCCTGGAGACAGAAAACAGATTTCATGGAAAGCAGCGGCTGGCAATGGCTTTTCAAAGCTACAGTTGGACTCATCTGGTATTTCAGCTGGTTTAATATCTCAAAAAGTAATACAAAGTTAAAGCATGCCATTTATTGTAGCTTCTTGCTGTTAGACATGATGATGCTTCTGGGCTTCTGGAGTTGGAAGGTGACCGAGTATGCAGGCTGCTGGACCTCTTTAAACCCTGCTGTAGTTATCCCAACACTACTAGGATTGTATATCATTGGAAATCTAGTGATGATGATGAACTACAAATGGTTTTATACTAGCTACAAACAGAAAACAGATGAACTCAGTAAAAAAATCAAAGAAGGTACATTTAAAAAAGCAATGCCATTAGGTTATAGCATTGAGACAGAAACTGTAGATGAAGTTCCTGGAGTTCTCCTTCGAAGT[A/T]AAATCATGGCAGCAGATTTCTGCTTTTAGTTCTTAATTCAATTGTACAAACCCTTCCCTATATCCAGTTTTGTTACTGTAAAATTTATAAACTGTTATAGACAATATACCTATTTTCATAATGGATTACTATCTTAGGAATAAAGCTGCAAAACCTGTCAGAGGGGAAGCATCTTTTTAAAAGGTACACTTTTATACCTTACAGGTGCACATTAGTATATAAAAGGTACAATGTGGTACTTTTAATGTACAATTTTATACATTTAGGGTACTATGAGGTACCCTTTTCTAAAGTCACAGGTTTGTACCTTTATTTCTGTGAGTGTTTGTGAGAATTGTTTACAAGACAAACACTATTTAGATGGCTGTGAAGGAGTGGTATCCTGATCAATGGCAATTTTTATATATTGTCTGCCTGTATCCTTTCTGTGATTTGATAATAATAAAGTTTTGAATCAATGGTTTTGCTGAATGTCTGTGTTTCTCTATAGATTGCATGAC

Associated Phenotype:

Not determined