ZMP

ENSDARG00000077867

Ensembl ID:

Human Orthologues:

PCDHB1, PCDHG@, PCDHGA1, PCDHGA10, PCDHGA11, PCDHGA12, PCDHGA3, PCDHGA5, PCDHGA6, PCDHGA7, PCDHGA8

Human Descriptions:

protocadherin beta 1 [Source:HGNC Symbol;Acc:8680]
protocadherin gamma cluster [Source:HGNC Symbol;Acc:8695]
protocadherin gamma subfamily A, 1 [Source:HGNC Symbol;Acc:8696]
protocadherin gamma subfamily A, 10 [Source:HGNC Symbol;Acc:8697]
protocadherin gamma subfamily A, 11 [Source:HGNC Symbol;Acc:8698]
protocadherin gamma subfamily A, 12 [Source:HGNC Symbol;Acc:8699]
protocadherin gamma subfamily A, 3 [Source:HGNC Symbol;Acc:8701]
protocadherin gamma subfamily A, 5 [Source:HGNC Symbol;Acc:8703]
protocadherin gamma subfamily A, 6 [Source:HGNC Symbol;Acc:8704]
protocadherin gamma subfamily A, 7 [Source:HGNC Symbol;Acc:8705]
protocadherin gamma subfamily A, 8 [Source:HGNC Symbol;Acc:8706]

Mouse Orthologue:

Pcdhb1

Mouse Description:

protocadherin beta 1 Gene [Source:MGI Symbol;Acc:MGI:2136730]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa42334	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa42334

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115147	Nonsense	74	805	1	1

Genomic Location (Zv9):

Chromosome 14 (position 2840317)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	2170234
GRCz11	14	2088585

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAAGACTGTTATCTCGTAAAGCTCGTATTGATGCTGAAGGTAACAGAAAA[C/T]GATATTGTGACATAAATCTGAACACTGGAGAGCTGACCGTAGCGGAGAGA

Long Flanking Sequence:

GTTCTTTTAACACTTAAAGCTGTCAGAAGCTTTAATGTCATGCAGTTTCTTTTTTTCAACTCACAGTGTCGCTGTTTAACTGCATAACCTTTACTCTGTTCAGTGCAAATGTCTCCACCCTGCTTACGCTAAAGAGCTGCCAGTTCCTCAGTTACAGAAAATCGTCGACGGTGGCAAGGCCACATTTCAAGCTGTTAGCCTGTTCTTTTATACATTTAATTGTACATTTGTTTCGTTTTTCGTGTTAATAGCAAGTTTTCCCTGGGATTCATTTTTGCCTAATGTCTTGGGCATTTCAAAAGCTCTGCTTTGCTGCTGAGATGTTCGTTCTTTTGTTCTTCGTGCTGATGGCGCACAGCGCTTATGGAGACGTGAGCTATTCTTTCCCGGAGGAGATGAAACGCGGATCTGTGATTGGAAATATAGCAAAGGATCTCGGACTCGATGTGAAAAGACTGTTATCTCGTAAAGCTCGTATTGATGCTGAAGGTAACAGAAAA[C/T]GATATTGTGACATAAATCTGAACACTGGAGAGCTGACCGTAGCGGAGAGAATCGACAGAGAAGGGCTTTGTGGAAAAAAAGCGTCATGCGTTCTTAAACAGGAGCTCGTGCTGGAAAATCCTTTAGAGCTGCATCGCTTTATTTTTAATATTGAGGACATTAATGATAATTCACCGCAATTTAAAGAAAATGTCATTAAATTTGAAATGCACGAGTTGGCAGTTAAAGGATCTCGTTATTTATTAGACGAGGCTCATGATGCGGATATTGGTATGAATTCAGTGCAGTCATATACAATTCAGAATAATGAACACTTTCTCCTTAGTGTAATAACGCGTCCAAATGGAAGAAAATATGGCGAACTCGTGCTGAATAAAGAGCTGGATCGTGAGCAGCAGAAAGAGGTGACTTTAATTCTGACTGCGGTAGACGGCGGGACTCCACCGAGATCAGGTACTGTAGCCATACACGTCACTGTGCTGGATGCTAATGATAATGCT

Associated Phenotype:

Not determined