ZMP

si:dkey-202m22.6

Ensembl ID:

ENSDARG00000036952

ZFIN IDs:

ZDB-GENE-091117-2, ZDB-GENE-091214-2

Description:

XK-related protein 7 [Source:RefSeq peptide;Acc:NP_001012252]

Human Orthologue:

XKR7

Human Description:

XK, Kell blood group complex subunit-related family, member 7 [Source:HGNC Symbol;Acc:23062]

Mouse Orthologue:

Xkr7

Mouse Description:

X Kell blood group precursor related family member 7 homolog Gene [Source:MGI Symbol;Acc:MGI:3526711

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37748	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa37749	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37748

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000053661	Essential Splice Site	240	560	2	3

Genomic Location (Zv9):

Chromosome 23 (position 31117095)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	30951985
GRCz11	23	30878516

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGCAGCTCAGCATTATGGTCCAGACCGGCCAGATTCTCCCTTTACAGGG[T/C]AAGTGTTGACAGCTATGATTAAAACCCACTCTCTACAAGTATGCTAGAAA

Long Flanking Sequence:

AACACTTTATATGGGCTGAATTTAAACAAACAAATTTAGTTGAGCATTGCTACATTTAATTGGTTTAAATTCAGCCTATATAAATTGTTTGCAACCACTTACCTTTAAAAAGTAAATATCCAATTTTTATTTTTTTATGGTTTGACATGGACTTGAAAATTATACATTGAATTTATATGCATAAACCATACTAAATGAAAGGAAAGCATTTTAAAACAACAAGCATTATGAAGTGAGCTTTAGTGATATTTGTGGAAATGATTTAAGGGCCCATACCATGTTTTCTTTCTGAATCTCAGGTATGTCCATGCCTTATATCTGGGTGTGCAGAGCCGCTGGCGTGGGGAGCACGAGCACAAACACTACTACTGGCGCACAATGTTTGAGAACGCTGATATCAGCATGCTGAGGCTGCTGGAGACCTTCCTGAAGAGCGCACCTCAGCTCGTCCTGCAGCTCAGCATTATGGTCCAGACCGGCCAGATTCTCCCTTTACAGGG[T/C]AAGTGTTGACAGCTATGATTAAAACCCACTCTCTACAAGTATGCTAGAAATAGTTGGCCCTGTATTATATTCACTGTATTCATATTTCATGTCTTGAGTATGCTGTAAAAATAGAATTATTGGTCACCTGTGGCATGGTTTTTCATTTATTTTGTTTTGCATTAGGTATGGAGGACTAGGAGAGCCAGTTAGAAATAAAATCAAGAATCAAATTATTAGTTTAATAATTGAAGCATAAAAATGTATATAAATAAATCCCAATTTAAGTGAACAAATTATGGACAAATAAATAGACATATTTGAATGTGTTTATATAAACTGTGCTTTTATATGTAATTTAATAAAGCAATAAAACAATGCATTTATTAATAGCTTTAAATGTATAAATAAATAGACAATTTTATAAATGTTTATTTAATTAATGTTTTAAAACTCTGATTAATCAAACAATAAAAAAGTAATTTCTAGATGATTTTAAATGCATTTAAATGCACAGTTTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37749

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000053661	Nonsense	349	560	3	3

Genomic Location (Zv9):

Chromosome 23 (position 31128569)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	30963459
GRCz11	23	30889990

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGGAGATCATCTACAACATGATGGTGGGCATTGTGTATATATTCTGCTG[G/A]TTCAGCGTTCGTGAGGGTCCCACGCGGGGCCGTCTTCTGCTGTACAGCCT

Long Flanking Sequence:

ATATGCAACATTATATCATTATAAGACATTATTAAAGTGATACTCTCCCTTAGTTTTGGTTAAATCAAGTGAGAATCTTTCTCCAGTGCAAATAAATGTAATTACTGTACCTCCTGTATTAACTCATTTGTTCTCTTTTCTCTCTGTCACTCTTATACTTCATTTGATCCAGGTCTGTCCGCGTCGGCCTCTCTAGTGTCTCTGGGCTGGATGATGGCGTCTTATCAGAAGGCATTGCGAGACTCTCGTGACGACAAGCTTCCCATGTCGTATAAAGCAGTGGTGGTGCACATGCTGTGGCATCTGTTCACCGTGGGAGCCCGCGCCATGGCTTTTGCCCTCTTCGTTTCCCTCTTCCAGCTCTACTTTGGCATTTTCATCGTGGCCCACTGGTGCGCCATGACCTTCTGGATCATCCAAGGCGAGACGGACTTCTGTATGTCCAAATGGGAGGAGATCATCTACAACATGATGGTGGGCATTGTGTATATATTCTGCTG[G/A]TTCAGCGTTCGTGAGGGTCCCACGCGGGGCCGTCTTCTGCTGTACAGCCTTATAATCTTGGCTGAAAACGTGGCTCTAACAGCTGTGTGGTACATATACCGCAGCCCGCGTACATCTGACTTTTACGCCGTGGTTGTGGTGTGTGTTGTGGCCTGTAGCTACGCTTTGGGCACATTTTTTATGTTTGTCTACTACTGCCTTTTACATCCTGATGGCCCTGTACCCGGGGCCTATCTTGGATGTTGTGGCGTGCAGGTGGGTGCTGTTTCAGATCCTTGTGTCTCGTCACCTACATCCGCTCCTCCTCTGGATGTGGTGAGCAGCCCTCCTCGGACTCTTCAGAGGACTAAAGGAATAGATTCAGTACCAATGGGAGACATCGGGGAAGTCTTTAAGATGCGGACCCTTAAGGCCTCTCGAAACGCGGCACCTCGCGTCACCCCAAGGACAGAGGGGCCGGTAATTCGTATCGACCTTCCCAGGAAACAGTACCCAGCCTG

Associated Phenotype:

Not determined