Busch Lab

ZMP

LOC560557

Ensembl ID:
ENSDARG00000015144
Human Orthologue:
SH2D4B
Human Description:
SH2 domain containing 4B [Source:HGNC Symbol;Acc:31440]
Mouse Orthologue:
Sh2d4b
Mouse Description:
SH2 domain containing 4B Gene [Source:MGI Symbol;Acc:MGI:1925182]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa11122 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa11122
Status:
Available for shipment
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Availability:
Order Allele From ZIRC
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Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000021301 Nonsense 281 424 7 9
Genomic Location (Zv9):
Chromosome 12 (position 30843280)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 29180217
GRCz11 12 29295119
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGAAACAAACAGGCATTTGATTGTCTTCATTGCTTTTCAGTCCTGTCTG[G/A]WTTCGTCCRACCAGACCGAACTCGCGWGAATCCATCATCCGCTGGTTTAA
Long Flanking Sequence:
GTCCGCCTGCTCTAATATAAAGTAGCTTATTTCTATTCAAATTCCTCCCTGCTTCCCACAGTGCGGCGCTCCAAGGCGGCAGATGAGGAGATGAAATGCAAGGCACGAAGGGCTAGAGATGAATACAAGCGGCAGTCTCTGCGGGCCGCTGAGAAGGGTCTGGTGGCTGGACTCAGTGGTCTGTTCCATAAGACACACCTGAATGGATCGGGTCACAACCGACGACACGGCACAGCCGCTGAACATTCATCTCCTCCAGCTGAGGCCAGCCATTCGCATGCAACCAGTGCTGGACAACTCACCTCAGGCCATTACAGGCACAGACAACACCATCGCTACAGCAGTCCAGTCACACAGTCGCTCACAGAATGGTAAAATCAATGCTGAGATCAATAATAAATGTTCTGGACAATACCTCTCACATACTCTGGCCTGTAATGCCACAATAAAGCGAAACAAACAGGCATTTGATTGTCTTCATTGCTTTTCAGTCCTGTCTG[G/A]ATTCGTCCAACCAGACCGAACTCGCGTGAATCCATCATCCGCTGGTTTAAGAAGGAGCAGAGGCCGAAACGAGCAGGTTATGAACGAAGCAGCAACACCATCGCACCCTGGTTTCACGGTAAAGAGAATCTTGAGGCCTATTCTCACCTCATGGCACCATGCAGCACTGTGACCTCTATACAGAAAAGCAGATGCAATGAGAGGACAATTTCAGGAATTTGTAAATGCATACCATTGAACAACAAAATGTGAACACAAAAGGACTTGTCATAAATGGTTTAAAAATATGGCACAATTTGACATTCTAAAGTTCACATTTTTTATAAATGACAGCAGATTTGACATCAAAAACCAAAAAAACTAATTCTAAGGTAAGTTTTGACACATGGCTGCTGGTTTAGGCTGGTTCTTTGCTGGTCAGAACCAGCTTAGAACCAACACATGAACAGCAAGGAAACAGCAAAACCAGCACATCACCAGCATAAACCAGCTTATGACCA
Associated Phenotype:
Not determined