ZMP

ENSDARG00000087121

Ensembl ID:

Human Orthologues:

PCDHA1, PCDHA10, PCDHA11, PCDHA12, PCDHA13, PCDHA2, PCDHA3, PCDHA4, PCDHA5, PCDHA6, PCDHA7, PCDHA8, PCDHA9

Human Descriptions:

protocadherin alpha 1 [Source:HGNC Symbol;Acc:8663]
protocadherin alpha 10 [Source:HGNC Symbol;Acc:8664]
protocadherin alpha 11 [Source:HGNC Symbol;Acc:8665]
protocadherin alpha 12 [Source:HGNC Symbol;Acc:8666]
protocadherin alpha 13 [Source:HGNC Symbol;Acc:8667]
protocadherin alpha 2 [Source:HGNC Symbol;Acc:8668]
protocadherin alpha 3 [Source:HGNC Symbol;Acc:8669]
protocadherin alpha 4 [Source:HGNC Symbol;Acc:8670]
protocadherin alpha 5 [Source:HGNC Symbol;Acc:8671]
protocadherin alpha 6 [Source:HGNC Symbol;Acc:8672]
protocadherin alpha 7 [Source:HGNC Symbol;Acc:8673]
protocadherin alpha 8 [Source:HGNC Symbol;Acc:8674]
protocadherin alpha 9 [Source:HGNC Symbol;Acc:8675]

Mouse Orthologue:

AC020968.2

Mouse Description:

protocadherin alpha-3 [Source:RefSeq peptide;Acc:NP_619603]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa42333	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa42333

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 > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114785	Nonsense	19	794	1	1

Genomic Location (Zv9):

Chromosome 14 (position 2723721)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	2291336
GRCz10	14	2295187
GRCz11	14	2209687
GRCz11	14	2213538

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGTGATGCACAGAAGGAGATCTGTCGTGGCTTGTTTTGTGCTCGCTGTTT[T/G]AGTGTGTTTCTGGGACGCGGCATCAGGGCAGCTCTCCTATTCTGTTTCTG

Long Flanking Sequence:

ACGAATAAAGTACATGCAAGCACAAAATAGCTTGGCAAACTTGCACCAACATTTTCTCACATATTGGACAAACTGAAATATCAATGATTTCTAATAGGCTAGTATTGTTTTTTTTTTTTTTTTTTTGAATGATAACTGTAATGATGATTTGTGATATTGGACTTTTTTTTTTTGTTGCTTTCAATTCATAAATCCGCTTGGTGTCACTATAGACCGTATCATTTGGTCTAATATTTCGTGTCTGGAAGCCCCTCCTGGTTCTAGTGGGGAGGGGATTTCACAGGGCTTTGTTTCAGAGAGACTGAACGTGTAACAGTGAGCGAAGGCCTCGTGTTGTGTCGTCGATAAAATGGGATGTTGTCTAATATTTCTTGATTCGCGTGGATGAACTTGGATTTTCTCTTTTGCTTTGTGGATAACTGCACTGGATTCAGTGGATGTCGCGATGTTCGTGATGCACAGAAGGAGATCTGTCGTGGCTTGTTTTGTGCTCGCTGTTT[T/G]AGTGTGTTTCTGGGACGCGGCATCAGGGCAGCTCTCCTATTCTGTTTCTGAGGAGGTGAGTCCGGGAACAACAGTGGGAAATCTCGCTAAGGATCTAAACCTGAATGTTCAGGAACTGGAGTCGCGCATGTTTCAGATTGTCACGGGAGCCAAGAAAAAATATTTCGAGGTAAATCTAAAAACTGGGTTTTTATATGTGAACGAAAGAATAGACAGAGAGGAGCTTTGCGCCAAAGCGCCCAAATGCACAGTCAGTGTAGAGGCAGTTATCAACAATCCATTAAAGCTCTATCAGATAGAAATCAATATTGTGGATGTAAACGATAATAAACCGACATTTAATTCAAAAACTCAATATTTAGATGTCGCTGAGAACACTTTACCCGGCGTAAAATTCCCTCTTTCTTATGCGTCTGATGCGGATGTAGGAAAAAACACAGTGAGCACCTATAAGTTAAGCCAAAATGAGTATTTTTCCTTAGCAGTGCACAAAGGAGAAG

Associated Phenotype:

Not determined